Valtrum TOPICAL ANALGESIC

CAMPHOR, MENTHOL, METHYL SALICYLATE TOPICAL HUMAN OTC DRUG

Valtrum TOPICAL ANALGESIC is an FDA drug label for the active ingredient CAMPHOR, MENTHOL, METHYL SALICYLATE manufactured by Laboratorios Quantium LLC administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260513.

Generic name
CAMPHOR, MENTHOL, METHYL SALICYLATE
Manufacturer
Laboratorios Quantium LLC
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
75849-031
Application
M017
Label effective
20260513

About this product

Valtrum TOPICAL ANALGESIC is an FDA-registered drug product whose active ingredient is CAMPHOR, MENTHOL, METHYL SALICYLATE. It is labelled by Laboratorios Quantium LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 75849-031, application M017, label effective 20260513. It is one of 13 FDA drug label records sharing the active ingredient CAMPHOR, MENTHOL, METHYL SALICYLATE. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing CAMPHOR, MENTHOL, METHYL SALICYLATE are most often described in connection with: temporary relief, minor aches, pains muscles, joints associated, simple backache, arthritis strains, bruises sprains. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredients Camphor 3% Menthol 3% Methyl salicylate 10%

Indications & Usage

Uses For the temporary relief of minor aches and pains of muscles and joints associated with • Simple Backache • Arthritis • Strains • Bruises • Sprains

Dosage & Administration

Directions Adult and Children 18 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 18 years of age: Consult a doctor.

Warnings

Warnings For external use only • Avoid contact with eyes and mucous membranes • Do not use otherwise than as directed. Caution: Discontinue use if excessive irritation of the skin develops. When using this product: • Do not bandage tightly • Do not apply to wounds or damaged skin. Stop use and ask a doctor if: • Conditions worsens • Symptoms persist for more than 7 days or clear up and occur again within a few days. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help, or contact a Poison Control Center right away.

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How products containing CAMPHOR, MENTHOL, METHYL SALICYLATE compare

FDA lists 13 drug label records with CAMPHOR, MENTHOL, METHYL SALICYLATE as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

Dosage formProductsManufacturerProducts
— — PT. EAGLE INDO PHARMA 2
— — Sinsin Pharmaceutical Co., Ltd. 2
— — Amerisource Bergen 1
— — Big 5 Nutrition LLC 1
— — Borden Company (Private) Limited 1

Frequently asked questions

What is Valtrum TOPICAL ANALGESIC used for?
Uses For the temporary relief of minor aches and pains of muscles and joints associated with • Simple Backache • Arthritis • Strains • Bruises • Sprains

Who makes Valtrum TOPICAL ANALGESIC?
Laboratorios Quantium LLC is the labeler of record for Valtrum TOPICAL ANALGESIC. 13 FDA label records share the active ingredient CAMPHOR, MENTHOL, METHYL SALICYLATE, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does Valtrum TOPICAL ANALGESIC come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Valtrum TOPICAL ANALGESIC prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing CAMPHOR, MENTHOL, METHYL SALICYLATE?
Yes. 13 FDA drug label records list CAMPHOR, MENTHOL, METHYL SALICYLATE as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has Valtrum TOPICAL ANALGESIC been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.