Vaporizing Colds Rub

Vaporizing Colds Rub is an FDA-registered drug product whose active ingredient is MENTHOL. It is labelled by Delon Laboratories (1990) Ltd taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 61734-030, application M012, label effective 20260618. It is one of 193 FDA drug label records sharing the active ingredient MENTHOL. 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.

Across FDA labelling, products containing MENTHOL are most often described in connection with: temporarily relieves, cough due, minor bronchial, irritation associated, cold inhaled, pains muscles. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses temporarily relieves: cough due to minor bronchial irritation associated with a cold or inhaled irritants cough associated with a cold minor aches and pains of muscles and joints

Directions see important warnings under "When using this product" adults and children 2 years and older: rub on the throat and chest in a thick layer cover with a warm, dry cloth if desired clothing should be loose about throat and chest to help vapors reach the nose and mouth use up to three times daily or as directed by a doctor children under 2 years of age: ask a doctor

Warnings For external use only; avoid contact with eyes. Do not use: by mouth on wounds or damaged skin in nostrils with tight bandages Ask a doctor before use if you have excessive phlegm (mucus) emphysema persistent or chronic cough asthma cough associated with smoking When using this product, do not heat microwave add to hot water or any container where heating water. May cause splattering and result in burns. Stop use and ask a doctor if muscle aches and pains worsen or persist for more than 7 days or clear up and occur again within a few days cough perists for more than 1 week, tends to recur, or is accompanied by fever, rash, or persistent headache. A persistent cough may be a sign of a serious condition. 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.

FDA lists 193 drug label records with MENTHOL 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 Vaporizing Colds Rub used for?
Uses temporarily relieves: cough due to minor bronchial irritation associated with a cold or inhaled irritants cough associated with a cold minor aches and pains of muscles and joints

Who makes Vaporizing Colds Rub?
Delon Laboratories (1990) Ltd is the labeler of record for Vaporizing Colds Rub. 193 FDA label records share the active ingredient MENTHOL, 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 Vaporizing Colds Rub 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 Vaporizing Colds Rub 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 MENTHOL?
Yes. 193 FDA drug label records list MENTHOL 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 Vaporizing Colds Rub 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.