Label: GOOD NEIGHBOR PHARMACY COLD THERAPY PAIN RELIEF PATCH- menthol patch
- NDC Code(s): 46122-751-45, 46122-751-50
- Packager: Amerisource Bergen
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 18, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
- Warnings
- When using this product
- Stop use and consult a doctor if
- If pregnant or breast-feeding
- Keep out of reach of children and pets
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Directions
Adults and children 12 years of age and over: Carefully remove backing from patch. Apply sticky side of patch to affected area. Wear one patch up to 8 hours. Repeat as necessary, but no more than 3 times daily. Discard patch after single use. Reseal pouch after opening. Children under 12 years of age: consult a physician.
- Other information
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Inactive Ingredient
aloe vera extract, arnica montana extract, boswellia carterii resin extract, carboxymethylcellulose sodium, diazolidinyl urea, dihydroxyaluminum aminoacetate, glycerin, green tea extract, iodopropynyl butylcarbamate, kaolin, mineral oil, petrolatum,
polyacrylic acid, polysorbate 80, povidone, propylene glycol, sodium polyacrylate, tartaric acid, titanium dioxide, water - Good Neighbor Pharmacy Cold Therapy Pain Relief Patch
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INGREDIENTS AND APPEARANCE
GOOD NEIGHBOR PHARMACY COLD THERAPY PAIN RELIEF PATCH
menthol patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:46122-751 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 5 g in 100 g Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL (UNII: 6DC9Q167V3) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) TARTARIC ACID (UNII: W4888I119H) POVIDONE (UNII: FZ989GH94E) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L) MINERAL OIL (UNII: T5L8T28FGP) WATER (UNII: 059QF0KO0R) POLYACRYLIC ACID (8000 MW) (UNII: 73861X4K5F) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) ALOE VERA LEAF (UNII: ZY81Z83H0X) DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6) GLYCERIN (UNII: PDC6A3C0OX) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) KAOLIN (UNII: 24H4NWX5CO) PETROLATUM (UNII: 4T6H12BN9U) POLYSORBATE 80 (UNII: 6OZP39ZG8H) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) GREEN TEA LEAF (UNII: W2ZU1RY8B0) BOSWELLIA SERRATA RESIN OIL (UNII: 5T1XCE6K8K) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:46122-751-50 1 g in 1 POUCH; Type 0: Not a Combination Product 04/01/2023 2 NDC:46122-751-45 5 in 1 CARTON 04/01/2023 2 1 g in 1 PATCH; 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 04/01/2023 Labeler - Amerisource Bergen (007914906) Establishment Name Address ID/FEI Business Operations Foshan Aqua Gel Biotech Co., Ltd. 529128763 manufacture(46122-751)