GOLD ICE Pain Relief

GOLD ICE Pain Relief is an FDA-registered drug product whose active ingredient is MENTHOL. It is labelled by Eden's Answers, Inc. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 72226-305, application M017, label effective 20231111. 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: temporary relief, minor aches, pains muscles, joints associated, simple backache, arthritis strains, bruises sprains. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses temporary relief of minor aches and pains of muscles and joints associated with: simple backache arthritis strains bruises sprains

Directions apply to affected area not more than 3 to 4 times daily Adult and children 12 years of age and over: consult a physician Children under 12 years of age:

Warnings: For external use only Keep away from fire or flame Flammable: When using this product do not apply to wounds or damaged skin Do not bandage tightly do not use with a heating pad avoid contact with the eyes or mucous membranes use only as directed Stop Use and ask a Doctor if condition worsens symptoms persist for more than 7 days or clears up and occur again within a few days. redness or skin irritation occurs 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 GOLD ICE Pain Relief used for?
Uses temporary relief of minor aches and pains of muscles and joints associated with: simple backache arthritis strains bruises sprains

Who makes GOLD ICE Pain Relief?
Eden's Answers, Inc. is the labeler of record for GOLD ICE Pain Relief. 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 GOLD ICE Pain Relief 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 GOLD ICE Pain Relief 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 GOLD ICE Pain Relief 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.