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White Flower Analgesic Balm Floral Scented

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Active ingredients
  • Camphor (synthetic) 5.4 g/100 mL
  • Menthol 13 g/100 mL
  • Methyl Salicylate 35.8 g/100 mL
Other brand names
Dosage form
Oil
Route
Topical
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2010
Label revision date
October 2, 2023
Drug Information (PDF)
Prescribing information, PDF file
Active ingredients
  • Camphor (synthetic) 5.4 g/100 mL
  • Menthol 13 g/100 mL
  • Methyl Salicylate 35.8 g/100 mL
Other brand names
Dosage form
Oil
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2010
Label revision date
October 2, 2023
Manufacturer
HOE HIN PAK FAH YEOW MANUFACTORY LTD
Registration number
M017
NDC root
48256-0011
Drug Information (PDF)
Prescribing information, PDF file
Packaging Info (2 NDCs)
Packaging & NDC Codes (2)

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

If you are a consumer or patient please visit this version.

Drug Overview

WHITE FLOWER ANALGESIC BALM FLORAL SCENTED is a topical product designed to provide temporary relief from minor aches and pains in muscles and joints. You can use it for various conditions, including simple backache, arthritis, strains, bruises, and sprains.

This balm is formulated to help soothe discomfort, making it a convenient option for those seeking relief from everyday muscle and joint pain.

Uses

If you're experiencing minor aches and pains in your muscles and joints, this medication can help provide temporary relief. It's effective for various conditions, including simple backaches, arthritis, strains, bruises, and sprains.

You can rely on this treatment to ease discomfort from these common issues, allowing you to get back to your daily activities with less pain. Remember, it's designed for short-term use to help manage these minor ailments.

Dosage and Administration

If you are an adult or a child aged 3 years and older, you can apply one to two drops of the medication directly to the affected area. Make sure to do this no more than 3 to 4 times a day, and gently massage the area to help the medication absorb better.

However, if you are under 3 years old or pregnant, it’s important not to use this medication. In these cases, you should consult a physician (a medical doctor) for advice on what to do. Always follow these guidelines to ensure safe and effective use of the medication.

What to Avoid

It's important to use this product safely and effectively. You should never apply it to irritated or damaged skin, or on any wounds. Always follow the directions provided, as using it in any other way can lead to complications.

While using this product, be careful to avoid contact with your eyes or mucous membranes, as this can cause irritation. Additionally, do not wrap the area tightly with a bandage, as this may lead to unwanted side effects. Remember, your safety is the priority, so adhere strictly to these guidelines.

Side Effects

This product is intended for external use only. You should stop using it and consult a doctor if your condition worsens, if symptoms last longer than 7 days, or if they clear up and then return within a few days. Additionally, seek medical advice if you experience excessive skin irritation, nausea, vomiting, abdominal discomfort, diarrhea, or a skin rash.

If you are using this product for arthritis pain, stop use and contact a doctor if the pain continues for more than 10 days, if you notice any redness, or if it is being used for a child under 12 years of age.

Warnings and Precautions

This product is for external use only, so please avoid applying it to any internal areas. To ensure safety, keep it out of reach of children to prevent accidental poisoning. If the product is swallowed, seek medical help immediately or contact a Poison Control Center.

You should stop using this product and call your doctor if your condition worsens, if symptoms last longer than 7 days, or if symptoms improve and then return within a few days. Additionally, seek medical advice if you experience excessive skin irritation, nausea, vomiting, abdominal discomfort, diarrhea, or a skin rash. If you are using it for arthritis pain, stop use if the pain lasts more than 10 days, if you notice any redness, or if it’s being used on children under 12 years of age.

Overdose

If you suspect an overdose, it's important to stay calm and take immediate action. While the specific signs of an overdose are not detailed, common symptoms can include unusual drowsiness, confusion, or difficulty breathing. If you notice any of these signs, or if you are unsure, seek medical help right away.

In case of an overdose, contact your local emergency services or go to the nearest hospital. It's crucial to provide them with as much information as possible about the substance taken and the amount, if known. Remember, acting quickly can make a significant difference in your health and safety.

Pregnancy Use

If you are pregnant or have a child under 3 years old, it is important to consult your physician before using this medication. Your healthcare provider can help you understand the potential risks and benefits, ensuring the safety of both you and your baby. Always prioritize professional guidance when it comes to medication during pregnancy.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to consult your physician before using this medication. The safety of this drug during lactation (the period of breastfeeding) has not been established, and it is unclear whether it can pass into breast milk. This means that there may be unknown risks to your nursing infant, so discussing your options with a healthcare professional is essential for your and your baby's well-being.

Pediatric Use

If you are considering using this medication for your child, it's important to know that it is not recommended for children under 3 years of age or for pregnant women. If your child is between 3 and 12 years old, you should consult a physician before use. For children aged 3 and older, you can apply one to two drops to the affected area, but make sure to do this no more than 3 to 4 times a day, and massage it gently into the skin.

Always prioritize your child's safety by following these guidelines closely. If you have any concerns or questions about using this medication, don't hesitate to reach out to your healthcare provider for advice.

Geriatric Use

When it comes to using this medication in older adults, there is no specific information available about dosage adjustments, safety concerns, or special precautions. This means that if you or a loved one is an older adult, it’s important to consult with a healthcare provider for personalized advice. They can help determine the best approach based on individual health needs and any other medications being taken. Always prioritize open communication with your healthcare team to ensure safe and effective treatment.

Renal Impairment

If you have kidney problems, it's important to know that there are no specific guidelines or dosage adjustments mentioned for your condition in the available information. This means that the standard recommendations for the medication do not include special monitoring or safety considerations tailored for patients with renal impairment (kidney issues).

Always consult your healthcare provider for personalized advice and to ensure that any medication you take is safe and appropriate for your situation. They can help determine the best course of action based on your kidney health.

Hepatic Impairment

If you have liver problems, it's important to know that the information provided does not include specific guidelines for dosage adjustments, special monitoring, or precautions related to your condition. This means that there are no tailored recommendations for how the medication may affect you differently due to your liver health.

Always consult your healthcare provider for personalized advice and to ensure that any treatment plan is safe and effective for your specific situation. They can help determine the best approach based on your liver function and overall health.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications or tests you may be taking. In this case, there are no known drug interactions or laboratory test interactions associated with the medication. However, always ensure that your healthcare provider is aware of all the medications you are using, as this helps them provide the best care tailored to your needs.

By discussing your full medical history and any other treatments, you can help prevent potential issues and ensure your safety.

Storage and Handling

To ensure the best performance of your product, it’s important to store it properly. Keep the container tightly sealed to protect its contents. Store it at or below 30º C (86º F) and away from direct sunlight, as excessive heat and light can affect its effectiveness.

When handling the product, always do so with care to maintain its integrity. Following these storage and handling guidelines will help ensure that you use the product safely and effectively.

Additional Information

You should apply one to two drops of the medication to the affected area, not more than 3 to 4 times a day, and gently massage it in. It's important to keep this medication out of reach of children to prevent accidental poisoning. If the medication is swallowed, seek medical help or contact a Poison Control Center immediately.

FAQ

What is WHITE FLOWER ANALGESIC BALM used for?

WHITE FLOWER ANALGESIC BALM is used for the temporary relief of minor aches and pains of muscles and joints, including simple backache, arthritis, strains, bruises, and sprains.

Who should not use this product?

Do not use this product on children under 3 years of age, pregnant women, or on irritated or damaged skin. Consult a physician if you are in these categories.

How should I apply WHITE FLOWER ANALGESIC BALM?

For adults and children 3 years and older, apply one to two drops to the affected area not more than 3 to 4 times daily and massage gently.

What should I do if my condition worsens?

Stop using the balm and ask a doctor if your condition worsens, symptoms persist for more than 7 days, or if excessive skin irritation occurs.

Is it safe to use WHITE FLOWER ANALGESIC BALM during pregnancy?

No, pregnant women should not use this product and should consult a physician.

What are the storage instructions for this balm?

Store WHITE FLOWER ANALGESIC BALM tightly sealed at or below 30º C (86º F), away from direct sunlight.

What should I do if I accidentally swallow the balm?

If swallowed, get medical help or contact a Poison Control Center right away.

Are there any warnings associated with this product?

Yes, it is for external use only. Avoid contact with eyes or mucous membranes and do not bandage tightly.

Packaging Info

Below are the non-prescription pack sizes of White Flower Analgesic Balm Floral Scented (camphor, menthol and methyl salicylate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for White Flower Analgesic Balm Floral Scented.
Details

Drug Information (PDF)

This file contains official product information for White Flower Analgesic Balm Floral Scented, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

White Flower Analgesic Balm is a topical formulation presented in a 0.338 fl oz (10 mL) container. The product features a floral scent and is designed for analgesic purposes. The National Drug Code (NDC) for this formulation is 48256-0011-1.

Uses and Indications

This drug is indicated for the temporary relief of minor aches and pains associated with muscles and joints. Specifically, it is effective for conditions such as simple backache, arthritis, strains, bruises, and sprains.

There are no teratogenic or nonteratogenic effects associated with this drug.

Dosage and Administration

For adults and children aged 3 years and older, the recommended dosage is one to two drops applied to the affected area, not exceeding 3 to 4 applications per day. It is advised to massage the area gently after application to enhance absorption.

Use of this product is contraindicated in children under 3 years of age and in pregnant women. In such cases, consultation with a physician is strongly recommended prior to use.

Contraindications

Use of this product is contraindicated in the following situations:

  • Application on irritated or damaged skin is prohibited due to the potential for exacerbating the condition.

  • Application on wounds is contraindicated to prevent further injury or infection.

  • The product must not be used in any manner other than as directed to ensure safety and efficacy.

Additionally, contact with the eyes or mucous membranes should be avoided, and tight bandaging is not recommended during use.

Warnings and Precautions

For external use only. It is imperative to keep this product out of reach of children to prevent accidental poisoning. In the event of ingestion, immediate medical assistance should be sought, or contact a Poison Control Center without delay.

Healthcare professionals should advise patients to discontinue use and consult a physician if any of the following occur: the condition worsens; symptoms persist for more than 7 days; symptoms resolve and then recur within a few days; excessive skin irritation develops; or gastrointestinal symptoms such as nausea, vomiting, abdominal discomfort, diarrhea, or skin rash manifest.

In cases where the product is used for arthritis-related pain, patients should be instructed to seek medical advice if pain persists for more than 10 days, if redness is observed, or if the product is being used in children under 12 years of age.

No specific laboratory tests are recommended for monitoring the use of this product.

Side Effects

Patients should be aware that the product is intended for external use only. In clinical practice, it is important to monitor for adverse reactions and to take appropriate action if any of the following conditions arise.

Patients are advised to stop using the product and consult a healthcare professional if any of the following occur: worsening of the condition, persistence of symptoms for more than 7 days, recurrence of symptoms after initial improvement within a few days, or development of excessive skin irritation. Additionally, if patients experience nausea, vomiting, abdominal discomfort, diarrhea, or a skin rash, they should seek medical advice.

For patients using the product for pain associated with arthritis, it is recommended to discontinue use and consult a doctor if pain persists for more than 10 days, if redness is present, or if the product is being used in children under 12 years of age.

Drug Interactions

No drug interactions or drug and laboratory test interactions have been identified in the available data. Therefore, no specific recommendations for dosage adjustments or monitoring are necessary at this time.

Packaging & NDC

Below are the non-prescription pack sizes of White Flower Analgesic Balm Floral Scented (camphor, menthol and methyl salicylate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for White Flower Analgesic Balm Floral Scented.
Details

Pediatric Use

Pediatric patients under 3 years of age and pregnant women should not use this product without consulting a physician. For adults and children aged 3 years and older, the recommended dosage is one to two drops applied to the affected area, not exceeding 3 to 4 times daily, with gentle massage.

In conditions affecting children under 12 years of age, the use of this product is not recommended.

Geriatric Use

There is no specific information regarding the use of this medication in geriatric patients, including dosage adjustments, safety concerns, or special precautions. Healthcare providers should exercise caution when prescribing this medication to elderly patients, as individual responses may vary. It is advisable to monitor these patients closely for any adverse effects or changes in efficacy.

Pregnancy

Pregnant women and children under 3 years of age should not use this medication without consulting a physician. The safety of this medication during pregnancy has not been established, and potential risks to fetal outcomes are not fully understood. Healthcare professionals are advised to evaluate the benefits and risks before prescribing this medication to women of childbearing potential. It is essential to consider alternative treatments and to provide appropriate counseling regarding the use of this medication during pregnancy.

Lactation

Lactating mothers are advised to consult a physician prior to using this medication. The safety of this medication during lactation has not been established, and the potential for excretion in breast milk is currently unknown. Therefore, caution is recommended when considering the use of this medication in nursing mothers.

Renal Impairment

Patients with renal impairment have not been specifically addressed in the available prescribing information. There are no dosage adjustments, special monitoring requirements, or safety considerations outlined for individuals with reduced kidney function. Healthcare professionals should exercise caution and consider the lack of data when prescribing to this patient population.

Hepatic Impairment

Patients with hepatic impairment have not been specifically studied in relation to the use of this medication. Consequently, there are no established dosage adjustments, special monitoring requirements, or precautions outlined for individuals with compromised liver function. It is recommended that healthcare providers exercise caution when prescribing this medication to patients with hepatic impairment, given the lack of data on its safety and efficacy in this population. Regular monitoring of liver function may be prudent in these cases, although specific parameters are not defined in the available information.

Overdosage

In the absence of specific information regarding overdosage, healthcare professionals are advised to exercise caution and adhere to general principles of management in cases of suspected overdose.

It is essential to monitor the patient closely for any potential symptoms that may arise, as the clinical presentation can vary depending on the substance involved and the individual patient's response. Common symptoms of overdose may include, but are not limited to, altered mental status, cardiovascular instability, respiratory distress, and gastrointestinal disturbances.

In the event of an overdose, immediate medical attention should be sought. Healthcare providers should initiate supportive care, which may include maintaining airway patency, providing supplemental oxygen, and monitoring vital signs. The use of activated charcoal may be considered if the patient presents within a suitable timeframe and if the ingestion was recent.

Furthermore, specific antidotes or treatments may be indicated based on the substance involved in the overdose. Consultation with a poison control center or a medical toxicologist is recommended to guide the management of the patient effectively.

Overall, vigilance and prompt intervention are critical in managing cases of suspected overdose, even in the absence of detailed information regarding specific overdosage effects.

Nonclinical Toxicology

Children under 3 years of age and pregnant women are advised against use and should consult a physician prior to administration. No specific non-teratogenic effects have been identified. Additionally, there are no detailed findings related to nonclinical toxicology or animal pharmacology and toxicology available.

Postmarketing Experience

Serious side effects have been reported voluntarily or through surveillance programs. Healthcare professionals and patients are encouraged to report any adverse events associated with the use of the product. Reports can be submitted using the designated phone number provided for this purpose.

Patient Counseling

Healthcare providers should advise patients to keep this medication out of reach of children to prevent accidental poisoning. It is important to emphasize the potential risks associated with ingestion by children.

In the event that the medication is swallowed, patients should be instructed to seek medical help immediately or contact a Poison Control Center for guidance. This prompt action is crucial to ensure the safety and well-being of the patient.

Storage and Handling

The product is supplied in a tightly sealed container to ensure its integrity. It should be stored at or below 30º C (86º F) and kept away from direct sunlight to maintain its efficacy and stability. Proper handling and storage conditions are essential to preserve the quality of the product.

Additional Clinical Information

The product is administered topically, with a recommended application of one to two drops to the affected area for adults and children aged 3 years and older, not exceeding 3 to 4 times daily. Gentle massage of the area is advised following application.

Clinicians should counsel patients to keep the product out of reach of children to prevent accidental poisoning. In the event of ingestion, patients should seek medical assistance or contact a Poison Control Center immediately.

Drug Information (PDF)

This file contains official product information for White Flower Analgesic Balm Floral Scented, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Data Generation & Sources

This page was automatically generated and is maintained by the AllDrugs AI Data-Science Team. It was built from the FDA Structured Product Label (DailyMed) for White Flower Analgesic Balm Floral Scented, retrieved by a validated AI data-extraction workflow.

All FDA-listed dosage forms and strengths are shown in the Packaging & NDC Codes section above. Regulatory status appears in the Summary Information panel above and was verified in the FDA National Drug Code directory and the NSDE NDC Directory daily file.

Note: an automated daemon monitors NSDE checksums; when the record for this NDC changes, the new file is pulled instantly and this page is refreshed.

No human clinician has reviewed this version.

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Primary FDA sources:

Orange Book data shown on this page are limited to Regulatory Status (Rx), Established Pharmacologic Class (EPC), and Mechanism of Action (MoA).

Regulatory data notice: Information on this page is reproduced verbatim from FDA public databases (NSDE, Orange Book, Purple Book, DailyMed SPL). NDA/ANDA drugs are FDA-approved, BLA biologics are FDA-licensed. Inclusion alone does not guarantee current market availability or imply FDA endorsement.

Medical disclaimer: This AI-generated content is provided for educational purposes only and does not constitute medical advice. Always consult a licensed healthcare professional for diagnosis or treatment decisions.