Blaster Pain Relief Stick

MENTHOL, METHYL SALICYLATE, CAMPHOR TOPICAL HUMAN OTC DRUG

Blaster Pain Relief Stick is an FDA drug label for the active ingredient MENTHOL, METHYL SALICYLATE, CAMPHOR manufactured by Kalahari Rose, LLC 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 20260807.

Generic name
MENTHOL, METHYL SALICYLATE, CAMPHOR
Manufacturer
Kalahari Rose, LLC
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
87917-001
Application
M017
Label effective
20260807

About this product

Blaster Pain Relief Stick is an FDA-registered drug product whose active ingredient is MENTHOL, METHYL SALICYLATE, CAMPHOR. It is labelled by Kalahari Rose, LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87917-001, application M017, label effective 20260807. 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, METHYL SALICYLATE, CAMPHOR are most often described in connection with: condition worsens, symptoms persist, dyas clear, days discontinue, consult doctor. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredient Purpose Methyl Salicylate 14% Topical Analgesic Menthol 4% Topical Analgesic Camphor 4% Topical analgesic

Indications & Usage

If condition worsens, or if symptoms persist for more than 7 dyas or clear up and return again withing a few days, discontinue use of this product and consult a doctor.

Dosage & Administration

Directions Adults and children 2 years of age and older: apply to affected area not more than 3-4 times daily. Children under 2 years of age: Do not use, consult a physician.

Warnings

Warnings For external use only Do not apply to wounds or damaged skin Avoid contact with eyes If pregnant, nursing, or under medical care, consult a physician before use.

Frequently asked questions

What is Blaster Pain Relief Stick used for?
If condition worsens, or if symptoms persist for more than 7 dyas or clear up and return again withing a few days, discontinue use of this product and consult a doctor.

Who makes Blaster Pain Relief Stick?
Kalahari Rose, LLC is the labeler of record for Blaster Pain Relief Stick.

What form does Blaster Pain Relief Stick 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 Blaster Pain Relief Stick 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 Blaster Pain Relief Stick 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.