Non-proprietary name

HEADACHE PATCH CUTANEOUS HUMAN OTC DRUG

Non-proprietary name is an FDA drug label for the active ingredient HEADACHE PATCH manufactured by Nanjing 3H Medical Products Co.,Ltd. administered by CUTANEOUS. 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 20260806.

Generic name
HEADACHE PATCH
Manufacturer
Nanjing 3H Medical Products Co.,Ltd.
Product type
HUMAN OTC DRUG
Route
CUTANEOUS
Dosage form
N/A
NDC
87915-789
Application
M017
Label effective
20260806

About this product

Non-proprietary name is an FDA-registered drug product whose active ingredient is HEADACHE PATCH. It is labelled by Nanjing 3H Medical Products Co.,Ltd. taken by cutaneous and marketed as a human otc drug product. Identifiers on file: NDC 87915-789, application M017, label effective 20260806. 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 HEADACHE PATCH are most often described in connection with: children years, older remove, backing paper, apply clean, dry skin, temples tension, points wear, affected area. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Menthol 5%

Indications & Usage

• adults and children 12 years of age and older: Remove backing paper, apply to clean dry skin (temples or tension points), wear up to 8 hours, and discard after use. • apply to affected area not more than 3 to 4 times daily

Dosage & Administration

Menthol 5%

Warnings

For external use only. When using this product use only as directed do not bandage tightly avoid contact with the eyes or on mucous membranes Do not use on wounds, damaged skin, rashes, swollen skin, or blistered areas with a heating pad or apply local heat to the area of use Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days you experience pain, swelling or blistering of the skin If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children and pets. Call a Poison Control Center immediately if overdose or accidental ingestion occurs.

Frequently asked questions

What is Non-proprietary name used for?
• adults and children 12 years of age and older: Remove backing paper, apply to clean dry skin (temples or tension points), wear up to 8 hours, and discard after use. • apply to affected area not more than 3 to 4 times daily

Who makes Non-proprietary name?
Nanjing 3H Medical Products Co.,Ltd. is the labeler of record for Non-proprietary name.

What form does Non-proprietary name come in?
administered by cutaneous. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Non-proprietary name 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.

Has Non-proprietary name 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.