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Valtrum Us Aerobic Sport Immediate Action

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This product has been discontinued

Active ingredients
  • Camphor (synthetic) 2.5 g/100 g
  • Menthol 2.5 g/100 g
  • Methyl Salicylate 10 g/100 g
Other brand names
Dosage form
Liquid
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2013
Label revision date
September 28, 2020
Active ingredients
  • Camphor (synthetic) 2.5 g/100 g
  • Menthol 2.5 g/100 g
  • Methyl Salicylate 10 g/100 g
Other brand names
Dosage form
Liquid
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2013
Label revision date
September 28, 2020
Manufacturer
Laboratorios Quantium LLC
Registration number
part348
NDC root
75849-200

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

Drug Overview

VALTRUM is a powerful external analgesic designed to provide immediate relief from minor aches and pains in muscles and joints. It is particularly effective for conditions such as rheumatism, muscle strain, sprains, bruises, and stiffness in the neck and shoulders. This thermoactive medication works by applying heat to the affected area, helping to soothe discomfort and promote relaxation.

Manufactured by Laboratorios Quantium, LLC, VALTRUM is distributed in the USA by QUANTIUMMED DISTRIBUTORS, INC. If you have any questions or need further information, you can reach out to them directly.

Uses

You can use this medication for the temporary relief of minor aches and pains in your muscles and joints. It is effective for conditions such as rheumatism, muscle strains, sprains, bruises, and stiffness in the neck and shoulders. If you're experiencing any of these discomforts, this medication may help alleviate your symptoms.

It's important to note that there are no reported teratogenic effects (which means it doesn't cause birth defects) associated with this medication, making it a safer option for those concerned about such risks.

Dosage and Administration

To use this medication, apply it directly to the area of your skin that is affected. It's important not to rub or massage the area after application, as this can interfere with how the medication works. You’ll notice that your skin absorbs the medication quickly, which is a good sign that it’s starting to take effect.

For best results, you should apply the medication every 6 hours, but remember not to exceed 4 applications in a single day. Following these guidelines will help ensure that you get the most benefit from your treatment.

What to Avoid

It's important to be aware of certain situations where you should not use this medication. You should avoid using it if you are pregnant or nursing, or if the patient is a child under 8 years old. Additionally, do not apply it with a heating pad or any external heat, as this can increase the risk of side effects.

Make sure to keep the medication away from your eyes and mucous membranes, and do not apply it to wounds or damaged skin. Lastly, avoid tightly bandaging the area where the medication is applied. Following these guidelines will help ensure your safety and the effectiveness of the treatment.

Side Effects

For your safety, this product is for external use only. You should stop using it and consult your doctor if you experience skin redness or excessive irritation. Additionally, if your condition worsens, or if symptoms persist for more than 7 days or return after clearing up, it's important to seek medical advice.

Warnings and Precautions

This product is for external use only, so please avoid applying it to any internal areas. If you are a parent, note that it should not be used on children under 8 years old. Additionally, if you are pregnant or nursing, or if you plan to use a heating pad or apply any external heat, it’s best to avoid this product.

You should stop using this product and contact your doctor if you notice any skin redness or excessive irritation, if your condition worsens, or if your symptoms last more than 7 days or return shortly after improving. If the product is swallowed, seek emergency medical help or contact a Poison Control Center immediately.

Overdose

If you suspect an overdose, it's important to stay calm and take immediate action. While there is no specific information available about the effects of an overdose for this medication, you should be aware of general signs that may indicate a problem. These can include unusual drowsiness, confusion, or difficulty breathing.

If you notice any of these symptoms or if you believe you have taken too much of the medication, seek medical help right away. Contact your healthcare provider or go to the nearest emergency room. It's always better to be safe and get checked out if you have any concerns about your health.

Pregnancy Use

If you are pregnant or nursing, it is important to avoid using this medication. The potential risks to your baby during pregnancy or while breastfeeding are significant, and it is best to prioritize your health and your child's safety. Always consult with your healthcare provider for guidance on safe treatment options during this time.

Lactation Use

If you are breastfeeding, it is important to know that this medication should not be used while you are nursing. Using it during this time could pose risks to your baby. Always consult with your healthcare provider for guidance on safe medications while breastfeeding to ensure the well-being of both you and your infant.

Pediatric Use

It is important to note that this medication should not be used in children under 8 years of age. If you are a parent or caregiver, please ensure that your child meets this age requirement before considering this treatment. Always consult with your healthcare provider for guidance tailored to your child's specific needs and circumstances.

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 healthcare providers may not have tailored guidelines for elderly patients.

If you or a loved one is an older adult considering this medication, it’s important to discuss any potential risks and benefits with your healthcare provider. They can help determine the best approach based on individual health needs and circumstances.

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 plan is safe and effective for your specific situation. They can help monitor your kidney health and make any necessary adjustments to your medications.

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 you are taking, even if there are no specific drug interactions or laboratory test interactions noted for your treatment. This ensures that your healthcare team can monitor your health effectively and make informed decisions about your care.

Always feel free to ask questions and share any other medications or supplements you might be using. This way, you can work together to ensure your treatment is safe and effective.

Storage and Handling

To ensure your safety and the effectiveness of the product, store it in a cool, dry place away from heat and flames, as it is flammable. Always check the bottle for an imprinted seal around the neck before use; do not use the product if this tamper-evident seal is missing, broken, or destroyed, as this indicates that the product may not be safe for use.

By following these simple guidelines, you can help maintain the integrity of the product and ensure your safety during handling.

Additional Information

No further information is available.

FAQ

What is VALTRUM used for?

VALTRUM is a powerful external analgesic used for the temporary relief of minor aches and pains of muscles and joints associated with conditions like rheumatism, muscle strain, sprains, bruises, and neck and shoulder stiffness.

How should I apply VALTRUM?

Apply VALTRUM directly to the affected area every 6 hours, but do not rub or massage it into the skin. Do not use more than 4 times daily.

Are there any contraindications for using VALTRUM?

Do not use VALTRUM in children under 8 years of age, if you are pregnant or nursing, or with a heating pad. Avoid contact with eyes and mucous membranes, and do not apply to wounds or damaged skin.

What should I do if I experience skin irritation while using VALTRUM?

Stop using VALTRUM and consult your doctor if you experience skin redness, excessive irritation, if your condition worsens, or if symptoms persist for more than 7 days.

Is VALTRUM flammable?

Yes, VALTRUM is flammable, so keep it away from heat and flame.

What should I do if I accidentally swallow VALTRUM?

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

Packaging Info

Below are the non-prescription pack sizes of Valtrum Us Aerobic Sport Immediate Action (camphor (synthetic) , menthol, methyl salicylate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Valtrum Us Aerobic Sport Immediate Action.
Details

Drug Information (PDF)

This file contains official product information for Valtrum Us Aerobic Sport Immediate Action, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

This product is a powerful analgesic designed for immediate action, specifically formulated for external use. It is marketed under the brand name Valtrum US and is produced by Laboratorios Quantium, LLC. The product is thermoactive, making it suitable for aerobic sports applications. Distribution within the United States is exclusively managed by Quantiummed Distributors, Inc., located in Miami, Florida. For inquiries, the company can be contacted via telephone at 305-514-9718 or 786-250-8995, or through email at quantiummed@gmail.com and quantiumlab@gmail.com.

Uses and Indications

This drug is indicated for the temporary relief of minor aches and pains of muscles and joints associated with rheumatism, muscle strain, sprains, bruises, and neck and shoulder stiffness.

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

Dosage and Administration

The medication should be applied directly to the affected area. It is important to avoid rubbing or massaging the area after application, as this may interfere with the absorption process. The skin will absorb the medication quickly, facilitating its therapeutic effects.

The recommended application frequency is every 6 hours, with a maximum of 4 applications per day. Healthcare professionals should ensure that patients adhere to this dosing schedule to optimize treatment outcomes.

Contraindications

Use is contraindicated in the following situations:

  • Children under 8 years of age due to safety concerns.

  • Pregnant or nursing individuals, as the effects on fetal or infant development are not established.

  • Concurrent use with a heating pad or application of external heat, which may increase the risk of adverse effects.

  • Contact with eyes or mucous membranes, as this may cause irritation.

  • Application to wounds or damaged skin, which could exacerbate the condition or lead to infection.

  • Tight bandaging of the area, as this may impede circulation and lead to complications.

Warnings and Precautions

For external use only. This product is contraindicated in children under 8 years of age. It is also not recommended for use during pregnancy or while nursing. Additionally, the application of external heat, such as with a heating pad, should be avoided while using this product.

Healthcare professionals should advise patients to discontinue use and consult a physician if any of the following occur: skin redness or excessive irritation, worsening of the condition, or if symptoms persist for more than 7 days or resolve and then recur within a few days.

In the event of accidental ingestion, immediate medical assistance should be sought, or contact with a Poison Control Center is recommended.

Side Effects

For external use only. Patients should discontinue use and consult a healthcare professional if they experience skin redness or excessive irritation of the skin. Additionally, if the condition worsens or if symptoms persist for more than 7 days, or clear up and then recur within a few days, it is advised to seek medical advice.

Drug Interactions

No specific drug interactions have been identified in the available data. Additionally, there are no reported interactions with laboratory tests. Therefore, no dosage adjustments or monitoring recommendations are necessary based on the current information.

Packaging & NDC

Below are the non-prescription pack sizes of Valtrum Us Aerobic Sport Immediate Action (camphor (synthetic) , menthol, methyl salicylate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Valtrum Us Aerobic Sport Immediate Action.
Details

Pediatric Use

Pediatric patients under 8 years of age should not be administered this medication. Safety and efficacy have not been established in this age group, and caution is advised when considering treatment options for younger children.

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. Monitoring for potential adverse effects and therapeutic efficacy is recommended in this population.

Pregnancy

Pregnant patients and those who are nursing should not use this medication. The potential risks associated with the use of this drug during pregnancy have not been established, and its safety profile in this population remains unclear. Therefore, healthcare professionals are advised to consider alternative treatments for women who are pregnant or breastfeeding.

Lactation

Lactating mothers are advised against the use of this medication while nursing. There is no available data on the excretion of this drug in human breast milk or its effects on breastfed infants. Therefore, caution is warranted, and alternative treatments should be considered for lactating 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 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

Do not use this product if pregnant or nursing. There are no specified non-teratogenic effects associated with the use of this product. Additionally, no nonclinical toxicology data or animal pharmacology and toxicology information has been provided.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients to keep this product out of reach of children to prevent accidental ingestion. Instruct patients that if the product is swallowed, they should seek medical help or contact a Poison Control Center immediately.

It is important to inform patients that this product is not recommended for use in children under 8 years of age. Additionally, patients who are pregnant or nursing should be cautioned against using this product.

Patients should be made aware that the product should not be used in conjunction with a heating pad or any external heat application. They should be instructed to stop using the product and consult a doctor if they experience skin redness or excessive irritation. Furthermore, patients should be advised to discontinue use and seek medical advice if their condition worsens, if symptoms persist for more than 7 days, or if symptoms clear up and then recur within a few days.

When using this product, patients must be reminded to follow the directions carefully. They should be cautioned to avoid contact with the eyes and mucous membranes, and not to apply the product to wounds or damaged skin. Lastly, patients should be advised against tightly bandaging the area where the product is applied.

Storage and Handling

This product is supplied in a container that features an imprinted tamper-evident seal around the neck. It is essential to ensure that this seal is intact before use; do not utilize the product if the seal is missing, broken, or destroyed.

Due to its flammable nature, the product must be stored away from heat sources and open flames to prevent any risk of ignition. Proper handling and storage conditions are crucial to maintain the integrity and safety of the product.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Valtrum Us Aerobic Sport Immediate Action, 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 Valtrum Us Aerobic Sport Immediate Action, 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.