Valtrum Topical Analgesic Roll On

Valtrum Topical Analgesic Roll On is an FDA-registered drug product whose active ingredient is SALICYLIC ACID MENTHOL CAMPHOR (NATURAL). It is labelled by LABORATORIOS QUANTIUM LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 75849-301, application M017, label effective 20231109. It is one of 2 FDA drug label records sharing the active ingredient SALICYLIC ACID MENTHOL CAMPHOR (NATURAL). 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.

DOSAGE & ADMINISTRATION Adults and children 18 years of age and older: Spray a thin layer over the affected area not more than 3 to 4 times daily. Children under 18 years of age: Consult a doctor.

WARNINGS For the 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.

FDA lists 2 drug label records with SALICYLIC ACID MENTHOL CAMPHOR (NATURAL) 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.

What is Valtrum Topical Analgesic Roll On used for?
No indications section is present in the FDA label on file for this product. Consult the prescribing information supplied with the medicine or ask a pharmacist.

Who makes Valtrum Topical Analgesic Roll On?
LABORATORIOS QUANTIUM LLC is the labeler of record for Valtrum Topical Analgesic Roll On. 2 FDA label records share the active ingredient SALICYLIC ACID MENTHOL CAMPHOR (NATURAL), 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 Roll On 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 Roll On 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 SALICYLIC ACID MENTHOL CAMPHOR (NATURAL)?
Yes. 2 FDA drug label records list SALICYLIC ACID MENTHOL CAMPHOR (NATURAL) 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 Roll On 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.