SUPER WHITE STUFF Pain Relief

MENTHOL TOPICAL HUMAN OTC DRUG

SUPER WHITE STUFF Pain Relief is an FDA drug label for the active ingredient MENTHOL manufactured by BLUE SPRING WELLNESS, L.L.C. 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 20231110.

Generic name
MENTHOL
Manufacturer
BLUE SPRING WELLNESS, L.L.C.
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
14448-302
Application
M017
Label effective
20231110

About this product

SUPER WHITE STUFF Pain Relief is an FDA-registered drug product whose active ingredient is MENTHOL. It is labelled by BLUE SPRING WELLNESS, L.L.C. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 14448-302, application M017, label effective 20231110. 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.

What it is used for

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

Active ingredients

Active Ingredient Menthol, USP 1.4% Purpose Topical Analgesic

Indications & Usage

Uses For the temporary relief of minor aches and pains associated with arthritis simple backahe sprains strains bruises

Dosage & Administration

Directions Apply to affected area not more than 3 to 4 times a days. before using for children under 12 for arthritic conditions and for all children under 2 years of age for all other uses. Consult a doctor

Warnings

Warnings: For external use only Do not use on wounded, damaged or irritated skin. When using this product avoid contact with eyes or mucous membranes. Do not bandage tightly Stop use and ask a doctor if you experience a rash and/or a reaction condition worsens or if symptoms persist for more than 10 days or clears up and occur again within a few days. If Pregnant or Breast-Feeding ask a health professional before use. Consult a doctor before use on children under 12 years of age if arthritis conditions are present. For all other listed uses, consult a doctor before use on children under 2 years of age. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

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How products containing MENTHOL compare

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.

Dosage formProductsManufacturerProducts
— — Reckitt Benckiser LLC 23
— — Mondelez Global LLC 6
— — BLUE SPRING WELLNESS, L.L.C. 5
— — Shanghai Chuangshi Medical Technology (Group) Co., Ltd. 5
— — Bestco 4

Frequently asked questions

What is SUPER WHITE STUFF Pain Relief used for?
Uses For the temporary relief of minor aches and pains associated with arthritis simple backahe sprains strains bruises

Who makes SUPER WHITE STUFF Pain Relief?
BLUE SPRING WELLNESS, L.L.C. is the labeler of record for SUPER WHITE STUFF 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 SUPER WHITE STUFF 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 SUPER WHITE STUFF 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 SUPER WHITE STUFF 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.

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.