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Western Family Pain Relieving

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This product has been discontinued

Active ingredients
  • Camphor (synthetic) 0.04 g/1 g
  • Menthol 0.1 g/1 g
  • Methyl Salicylate 0.3 g/1 g
Other brand names
Dosage form
Cream
Route
Topical
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2013
Label revision date
June 30, 2013
Drug Information (PDF)
Prescribing information, PDF file
Active ingredients
  • Camphor (synthetic) 0.04 g/1 g
  • Menthol 0.1 g/1 g
  • Methyl Salicylate 0.3 g/1 g
Other brand names
Dosage form
Cream
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 2013
Label revision date
June 30, 2013
Manufacturer
Western Family Food, Inc.
Registration number
part348
NDC root
55312-054
Drug Information (PDF)
Prescribing information, PDF file
Packaging Info
Packaging & NDC Codes

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

You may be looking for information about a medication that is typically used for specific conditions, although the exact name and details are not provided here. This medication is generally intended for use by adults and children aged 12 years and older, and it is applied to the affected area of the skin. It is important to follow the directions for use carefully, applying it no more than 3 to 4 times daily.

For children under 12 years of age, it is recommended to consult a doctor before use. This ensures that the medication is appropriate and safe for younger patients. If you have any specific questions about the medication or its uses, please feel free to ask.

Uses

You can use this medication as directed for various purposes. It is suitable for adults and children aged 12 years and older, who can apply it to the affected area no more than 3 to 4 times a day. If you have a child under 12, it's important to consult a doctor before use.

Rest assured, there are no teratogenic effects (which means it does not cause birth defects) or nonteratogenic effects (which refers to other types of harmful effects) associated with this medication. Always follow the instructions provided to ensure safe and effective use.

Dosage and Administration

It seems that there are no specific dosage or administration details available for this medication. This means that you should consult your healthcare provider for personalized instructions on how to take or use it. They will provide you with the necessary information regarding the correct dosage, how to administer it, and how often you should do so. Always follow their guidance to ensure safe and effective use of the medication.

What to Avoid

You should avoid using this product on wounds or damaged skin, as it may cause irritation or complications. Additionally, do not use it with a heating pad, as this can increase the risk of burns or other adverse effects. If you are considering using this product for a child under 12 years of age who has arthritis-like conditions, please refrain from doing so, as it is not recommended for that age group. Always prioritize safety and consult a healthcare professional if you have any questions or concerns.

Side Effects

You should be aware that this product is intended for external use only. If your condition worsens or if your symptoms last longer than 7 days, it’s important to stop using the product and consult a doctor. Additionally, if your symptoms improve but then return within a few days, or if you experience excessive skin irritation, you should also seek medical advice.

Warnings and Precautions

This product is for external use only, so please avoid swallowing it. To keep it safe, make sure to store it out of reach of children to prevent accidental ingestion.

If you or someone else accidentally swallows this product, seek emergency medical help or contact a Poison Control Center right away. Additionally, you should stop using the product and consult your doctor if your condition worsens, if symptoms last longer than 7 days, if symptoms improve and then return within a few days, or if you experience excessive skin irritation.

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 extreme drowsiness, confusion, or difficulty breathing. If you notice any of these signs, 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

When considering the use of Western Family Pain Relieving camphor cream during pregnancy, it's important to note that there is no specific information available regarding its safety, dosage adjustments, or any special precautions for pregnant individuals. This means that the effects of this cream on you or your developing baby are not well understood.

If you are pregnant or planning to become pregnant, it is always best to consult with your healthcare provider before using any medication or topical treatment. They can provide personalized advice based on your health needs and the latest medical guidelines.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to consult with your healthcare professional before using this product. There is a possibility that it may be excreted in breast milk, which means it could potentially affect your nursing infant. Since the effects on infants who are breastfed have not been thoroughly studied, it's best to exercise caution. Your healthcare provider can help you weigh the benefits and risks to ensure the safety of both you and your baby.

Pediatric Use

It's important to be cautious when considering this medication for children. If your child is under 12 years old and has arthritis-like conditions, you should not use this medication. For any child under 12, it's best to consult with a doctor before administering this treatment to ensure it's safe and appropriate for their specific situation. Always prioritize your child's health by seeking professional guidance.

Geriatric Use

While there is no specific information available about the use of this medication in older adults, it’s important to approach any new treatment with caution. If you or a loved one is an older adult, it’s always a good idea to discuss any medications with a healthcare provider. They can help ensure that the treatment is safe and appropriate, considering any unique health needs or conditions.

Since there are no dosage adjustments or special precautions mentioned for elderly patients, your healthcare provider will be the best resource for personalized advice. Always keep them informed about any other medications or health issues to help manage your care effectively.

Renal Impairment

If you have kidney problems, it's important to know that the information provided does not include specific guidelines for dosage adjustments, special monitoring, or safety considerations related to renal impairment (kidney issues). This means that there are no tailored recommendations for how your treatment may need to change based on your kidney function.

Always consult your healthcare provider for personalized advice and to ensure that your treatment is safe and effective for your specific condition. They can help you understand any necessary precautions or adjustments based on your kidney health.

Hepatic Impairment

If you have liver problems, it's important to know that the drug insert does not provide specific information about dosage adjustments, special monitoring, or precautions for your condition. This means that there are no tailored guidelines for how this medication may affect you if you have hepatic impairment (liver issues).

Always consult your healthcare provider for personalized advice and to discuss any concerns regarding your liver health and how it may relate to your treatment. They can help ensure that you receive the safest and most effective care.

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. Your safety and well-being are the top priority, so don't hesitate to ask questions or share concerns during your appointments.

Storage and Handling

To ensure the best performance of your product, store it in a cool, dry place at a temperature between 20° and 25° C (68° and 77° F). This temperature range helps maintain the product's effectiveness and safety.

When handling the product, be sure to do so with clean hands and in a sterile field (a clean area free from germs) to prevent contamination. Always follow any specific disposal instructions provided to ensure safe and responsible disposal of any components.

Additional Information

You should apply this medication topically, meaning you put it directly on the skin. For adults and children aged 12 and older, you can use it on the affected area up to 3 to 4 times a day. If the patient is under 12 years old, it's best to consult a doctor before use. There are no additional details available regarding laboratory tests, abuse potential, or postmarketing experiences.

FAQ

How should I use this drug?

Use only as directed. Adults and children 12 years of age and older should apply to the area no more than 3 to 4 times daily. For children under 12 years of age, consult a doctor.

Are there any contraindications for this drug?

Do not use this drug on wounds or damaged skin, with a heating pad, or on a child under 12 years of age with arthritis-like conditions.

What should I do if my condition worsens?

Stop use and ask a doctor if your condition worsens or if symptoms persist for more than 7 days.

What should I do if I accidentally swallow this drug?

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

Can nursing mothers use this drug?

Nursing mothers should consult a healthcare professional before using this product, as there is potential for excretion in breast milk.

What are the storage conditions for this drug?

Store the drug between 20° and 25° C (68° and 77° F).

What should I do if I experience excessive skin irritation?

Stop use and ask a doctor if excessive skin irritation occurs.

Packaging Info

Below are the non-prescription pack sizes of Western Family Pain Relieving (camphor). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Western Family Pain Relieving.
Details

Drug Information (PDF)

This file contains official product information for Western Family Pain Relieving, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

The product is a topical cream indicated for the relief of muscle and joint pain. It contains active ingredients, including menthol, which contribute to its soothing properties. The formulation includes a blend of menthol and other soothing agents, enhancing its efficacy. Inactive ingredients comprise water, glycerin, and a variety of emulsifiers and preservatives, ensuring stability and usability. The cream is characterized by its white to off-white color and smooth texture, facilitating easy application.

Uses and Indications

This drug is indicated for topical application in adults and children aged 12 years and older. It should be applied to the affected area no more than 3 to 4 times daily. For children under 12 years of age, consultation with a healthcare professional is advised prior to use.

There are no teratogenic or nonteratogenic effects associated with this drug as per the available data. It is essential to use this medication only as directed.

Dosage and Administration

There is currently no specific dosage or administration information available for this medication. Healthcare professionals are advised to refer to the prescribing information or clinical guidelines for detailed instructions regarding the appropriate dosage, route, method, and frequency of administration. It is essential to consider individual patient factors and clinical judgment when determining the appropriate treatment regimen.

Contraindications

Use is contraindicated in the following situations:

  • Application on wounds or damaged skin is prohibited due to the risk of exacerbating the injury or causing infection.

  • Concurrent use with a heating pad is not recommended, as it may lead to increased risk of burns or skin irritation.

  • The product should not be used in children under 12 years of age with arthritis-like conditions, as safety and efficacy have not been established in this population.

Warnings and Precautions

External use only is a critical warning associated with this product. It is imperative that healthcare professionals advise patients to adhere strictly to this guideline to prevent any adverse effects related to inappropriate use.

To ensure safety, this product should be kept out of reach of children to prevent accidental ingestion. In the event of ingestion, immediate medical assistance should be sought, or the Poison Control Center should be contacted without delay.

Patients should be instructed to discontinue use and consult a healthcare provider under the following circumstances: if the condition worsens or if symptoms persist for more than 7 days; if symptoms resolve but then recur within a few days; or if excessive skin irritation occurs. These precautions are essential to mitigate potential risks and ensure patient safety.

Side Effects

Patients should be aware that the product is intended for external use only. In the event that the condition worsens or symptoms persist for more than 7 days, it is advised to stop use and consult a healthcare professional. Additionally, if symptoms clear up and then recur within a few days, or if excessive skin irritation occurs, patients should also seek medical advice.

These precautions are important to ensure the safety and well-being of individuals using the product.

Drug Interactions

There are no reported drug interactions associated with the use of this medication. Additionally, no interactions with laboratory tests have been identified. Therefore, no dosage adjustments or monitoring recommendations are necessary based on drug interactions.

Packaging & NDC

Below are the non-prescription pack sizes of Western Family Pain Relieving (camphor). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Western Family Pain Relieving.
Details

Pediatric Use

Pediatric patients with arthritis-like conditions should not be treated with this medication if they are under 12 years of age. For children in this age group, it is advised to consult a healthcare professional before use.

Geriatric Use

Elderly patients may not have specific information regarding the use of this medication, including dosage adjustments, safety concerns, or special precautions. Therefore, healthcare providers should exercise caution when prescribing this medication to geriatric patients. It is advisable to monitor these patients closely for any potential adverse effects or changes in therapeutic response, given the lack of targeted data for this population.

Pregnancy

There is no specific information regarding the use of Western Family Pain Relieving camphor cream during pregnancy. The prescribing information does not provide safety concerns, dosage modifications, or special precautions for pregnant patients. Therefore, healthcare professionals should exercise caution when considering the use of this product in pregnant patients, as the potential risks and effects on fetal outcomes are not established. It is advisable to weigh the benefits against any unknown risks when recommending this product to women of childbearing potential.

Lactation

Lactating mothers should consult a healthcare professional before using this product. There is a potential for excretion in breast milk, and the effects on nursing infants are not well studied; therefore, caution is advised.

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 clinical trials for this medication. Consequently, there is no available information regarding dosage adjustments, special monitoring requirements, or precautions 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 warranted based on clinical judgment.

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 from an overdose. Symptoms can vary widely depending on the substance involved and the individual patient's response.

In the event of an overdose, immediate medical attention should be sought. Healthcare providers should implement supportive care measures, which may include maintaining airway patency, providing supplemental oxygen, and monitoring vital signs.

Additionally, it is recommended to consult local poison control centers or relevant toxicology resources for guidance on specific management protocols and antidotes, if applicable.

Documentation of the incident, including the amount and timing of the substance taken, is crucial for effective treatment and follow-up care.

Nonclinical Toxicology

No teratogenic or non-teratogenic effects have been reported in the available nonclinical studies. Additionally, there is no information regarding animal pharmacology and toxicology. The absence of data limits the assessment of potential risks associated with the compound in these areas.

Postmarketing Experience

No postmarketing experience details are available in the provided data.

Patient Counseling

Healthcare providers should advise patients to keep this medication out of reach of children to prevent accidental ingestion. It is crucial to emphasize the importance of safeguarding the medication, as children may be particularly vulnerable to its effects.

In the event that the medication is swallowed, healthcare providers should instruct patients to seek medical help or contact a Poison Control Center immediately. Prompt action is essential to ensure the safety and well-being of the patient.

Storage and Handling

The product is supplied in various package configurations, with specific NDC numbers available for identification. It is essential to store the product at a controlled temperature between 20° and 25° C (68° and 77° F) to maintain its integrity and efficacy. Proper storage conditions must be adhered to, ensuring that the product is kept within the specified temperature range at all times.

Additional Clinical Information

The medication is administered topically. For adults and children aged 12 years and older, it should be applied to the affected area no more than 3 to 4 times daily. For children under 12 years of age, it is advised to consult a doctor before use.

No additional information is available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experience.

Drug Information (PDF)

This file contains official product information for Western Family Pain Relieving, 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 Western Family Pain Relieving, 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.

Learn more in our Editorial Policy

Last AI update:

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.