Label: THE GOO MEDICATED PAIN RELIEF- methyl salicylate, menthol, camphor gel
- NDC Code(s): 82503-101-11
- Packager: APSM PERFORMANCE, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 19, 2024
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- ACTIVE INGREDIENTS
- PURPOSE
- USES
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
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INACTIVE INGREDIENTS
1,2-Hexanediol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Caprylhydroxamic Acid, Capryloyl Glycerin/Sebacic Acid Copolymer, Dimethyl Isosorbide, Menthyl Ethylamido Oxalate, Propanediol, Steareth-2, Steareth-21, Stearyl Alcohol, Stearyl Glycyrrhetinate, Vanillyl Butyl Ether, Water, Xanthan Gum, Blue 1, Yellow 5, Green 3
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INGREDIENTS AND APPEARANCE
THE GOO MEDICATED PAIN RELIEF
methyl salicylate, menthol, camphor gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82503-101 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 30 g in 100 mL MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM 10 g in 100 mL CAMPHOR OIL (UNII: 75IZZ8Y727) (CAMPHOR OIL - UNII:75IZZ8Y727) CAMPHOR OIL 4 g in 100 mL Inactive Ingredients Ingredient Name Strength CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T) XANTHAN GUM (UNII: TTV12P4NEE) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) PROPANEDIOL (UNII: 5965N8W85T) DIMETHYL ISOSORBIDE (UNII: SA6A6V432S) CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36) STEARYL GLYCYRRHETINATE (UNII: 3YYE6VJS0P) FD&C YELLOW NO. 5 FREE ACID (UNII: 6TP696149N) FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S) STEARETH-2 (UNII: V56DFE46J5) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) WATER (UNII: 059QF0KO0R) STEARETH-21 (UNII: 53J3F32P58) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) MENTHYL ETHYLAMIDO OXALATE (UNII: G2MB8B7PSM) VANILLYL BUTYL ETHER (UNII: S2ULN37C9R) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82503-101-11 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/30/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 04/30/2022 Labeler - APSM PERFORMANCE, LLC (118493671)