Label: FOOT WORKS ARTHRITIS ACHY FOOT AND MUSCLE- methyl salicylate cream
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Updated January 1, 2019
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- ACTIVE INGREDIENT
- INDICATIONS & USAGE
For external use only
When using this product
• use only as directed
• avoid contact with the eyes or mucous membranes. If contact occurs, flush thoroughly with water.
• do not apply to wounds, damaged or irritated skin
• do not bandage
• do not use with a heating pad. The application of external heat, such as an electric heating pad, may result in excessive skin irritation or skin burn.
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
- DOSAGE & ADMINISTRATION
WATER/EAU, C12-15 ALKYL BENZOATE, GLYCERIN, ISOPROPYL PALMITATE, GLUCOSAMINE HCL, SODIUM CHONDROITIN SULFATE, ALGAE EXTRACT, YEAST EXTRACT/EXTRAIT DE LEVURE, POLYACRYLAMIDE, STEARETH-2, C13-14 ISOPARAFFIN, GLYCERYL STEARATE, PHENOXYETHANOL, STEARETH- 20, MENTHOL, METHYLPARABEN, LAURETH-7, CITRIC ACID, GLYCOLIC ACID, UREA, POTASSIUM HYDROXIDE.
- PRINCIPAL DISPLAY PANEL
INGREDIENTS AND APPEARANCE
FOOT WORKS ARTHRITIS ACHY FOOT AND MUSCLE
methyl salicylate cream
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10096-0004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 250 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10096-0004-1 75 mL in 1 TUBE; Type 0: Not a Combination Product 05/30/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 05/30/2012 Labeler - New Avon LLC (080143520)