BRONSON SOOTHE Pain Relief
BRONSON SOOTHE Pain Relief is an FDA drug label for the active ingredient CAPSAICIN manufactured by BRONSON NUTRITIONALS, 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 20231106.
Generic: CAPSAICIN
Manufacturer: BRONSON NUTRITIONALS, LLC
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 83158-387
Application: M017
Effective: 20231106
Active Ingredients: ACTIVE INGREDIENT Capsaicin 0.025% PURPOSE External Analgesic
Indications & Usage
USES: For temporary relief of minor aches and pains of the muscles and joints associted with simple backache, arthritis, strains, bruises and sprains.
Dosage & Administration
DIRECTIONS: Apply directly to affected area. Do not use more than four times per day.
Contraindications
Not available.
Warnings
WARNINGS For external use only. Avoid contact with eyes. Do not apply to open wounds or damaged skin. If symtoms persist for more than seven days, discontinue use and consult physician. Keep out of reach of children. If swallowed, contact physician. Do not bandage tightly . If pregnant or breast feeding, contact physician prior to use.
Adverse Reactions
Not available.
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