ANTIPHLAMINE

L-MENTHOL, L-CAMPHOR, METHYL SALICYLATE TOPICAL HUMAN OTC DRUG

ANTIPHLAMINE is an FDA drug label for the active ingredient L-MENTHOL, L-CAMPHOR, METHYL SALICYLATE manufactured by Masaem Company 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 20260716.

Generic name
L-MENTHOL, L-CAMPHOR, METHYL SALICYLATE
Manufacturer
Masaem Company
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
87538-0004
Application
M017
Label effective
20260716

About this product

ANTIPHLAMINE is an FDA-registered drug product whose active ingredient is L-MENTHOL, L-CAMPHOR, METHYL SALICYLATE. It is labelled by Masaem Company taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87538-0004, application M017, label effective 20260716. It is one of 2 FDA drug label records sharing the active ingredient L-MENTHOL, L-CAMPHOR, 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 L-MENTHOL, L-CAMPHOR, METHYL SALICYLATE are most often described in connection with: years age, affected area, times daily, consult doctor. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

L-Menthol L-Camphor Methyl Salicylate

Indications & Usage

Adults and children 2 years of age and over: apply to the affected area no more than 3 to 4 times daily. Children under 2 years of age: consult a doctor

Dosage & Administration

for external use only

Warnings

use only as directed do not bandage tightly or use with a healing pad avoid contact with the eyes and mucous membranes do not apply to wounds or damaged skin flammable

How products containing L-MENTHOL, L-CAMPHOR, METHYL SALICYLATE compare

FDA lists 2 drug label records with L-MENTHOL, L-CAMPHOR, 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
— — Lydia Co., Ltd. 1
— — Masaem Company 1
— — — —
— — — —
— — — —

Frequently asked questions

What is ANTIPHLAMINE used for?
Adults and children 2 years of age and over: apply to the affected area no more than 3 to 4 times daily. Children under 2 years of age: consult a doctor

Who makes ANTIPHLAMINE?
Masaem Company is the labeler of record for ANTIPHLAMINE. 2 FDA label records share the active ingredient L-MENTHOL, L-CAMPHOR, 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 ANTIPHLAMINE 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 ANTIPHLAMINE 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 L-MENTHOL, L-CAMPHOR, METHYL SALICYLATE?
Yes. 2 FDA drug label records list L-MENTHOL, L-CAMPHOR, 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 ANTIPHLAMINE 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.