Label: PAIN RELIEVER CREAM- menthol 10%, methyl salicylate 15% cream
- NDC Code(s): 69396-151-01
- Packager: Trifecta Pharmaceuticals USA, LLC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 6, 2024
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- Active Ingredient
- Active Ingredient
- PURPOSE
- INDICATIONS & USAGE
- Warnings
- Stop Use and ask a doctor
- Ask a doctor before use
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- Keep out of the reach of Children
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- Inactive Ingredients
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INGREDIENTS AND APPEARANCE
PAIN RELIEVER CREAM
menthol 10%, methyl salicylate 15% creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69396-151 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 10 g in 100 g METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 15 g in 100 g Inactive Ingredients Ingredient Name Strength POLYSORBATE 80 (UNII: 6OZP39ZG8H) TROLAMINE (UNII: 9O3K93S3TK) PROPYLPARABEN (UNII: Z8IX2SC1OH) CARBOMER 940 (UNII: 4Q93RCW27E) CETYL ALCOHOL (UNII: 936JST6JCN) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) METHYLPARABEN (UNII: A2I8C7HI9T) WATER (UNII: 059QF0KO0R) STEARIC ACID (UNII: 4ELV7Z65AP) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69396-151-01 1 in 1 BOX 03/06/2024 1 114 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 03/06/2024 Labeler - Trifecta Pharmaceuticals USA, LLC. (079424163)