SINSIN HANBANG FLEX

CAMPHOR, MENTHOL TOPICAL HUMAN OTC DRUG

SINSIN HANBANG FLEX is an FDA drug label for the active ingredient CAMPHOR, MENTHOL manufactured by Sinsin Pharmaceutical co., ltd. 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 20260521.

Generic name
CAMPHOR, MENTHOL
Manufacturer
Sinsin Pharmaceutical co., ltd.
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
55264-117
Application
M017
Label effective
20260521

About this product

SINSIN HANBANG FLEX is an FDA-registered drug product whose active ingredient is CAMPHOR, MENTHOL. It is labelled by Sinsin Pharmaceutical co., ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 55264-117, application M017, label effective 20260521. It is one of 10 FDA drug label records sharing the active ingredient CAMPHOR, 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.

What it is used for

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

Active ingredients

Uses Uses For temporary relief of minor aches and pains of muscles and joints associated with: ■ Arthritis ■ Simple backache ■ Strains ■ Sprains ■ Bruises

Indications & Usage

INDICATIONS Uses For temporary relief of minor aches and pains of muscles and joints associated with: ■ Arthritis ■ Simple backache ■ Strains ■ Sprains ■ Bruises

Dosage & Administration

Dosage & Administration section Adults and children 12 years of age and over: ■ Clean and dry affected area ■ Remove patch from film ■ Apply to affected area not more than 3 or 4 times daily ■ Remove patch from the skin after at most 8 hour application Children under 12 years of age: ■ Consult a doctor

Warnings

Warnings Warnings For external use only

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How products containing CAMPHOR, MENTHOL compare

FDA lists 10 drug label records with CAMPHOR, 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.

Dosage formProductsManufacturerProducts
— — Active and Innovative Inc. 3
— — PT. EAGLE INDO PHARMA 2
— — Active and Innovative 1
— — Borden Company (Private) Limited 1
— — Chattem, Inc. 1

Frequently asked questions

What is SINSIN HANBANG FLEX used for?
INDICATIONS Uses For temporary relief of minor aches and pains of muscles and joints associated with: ■ Arthritis ■ Simple backache ■ Strains ■ Sprains ■ Bruises

Who makes SINSIN HANBANG FLEX?
Sinsin Pharmaceutical co., ltd. is the labeler of record for SINSIN HANBANG FLEX. 10 FDA label records share the active ingredient CAMPHOR, 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 SINSIN HANBANG FLEX 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 SINSIN HANBANG FLEX 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?
Yes. 10 FDA drug label records list CAMPHOR, 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 SINSIN HANBANG FLEX 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.