Label: WALGREENS COLD THERAPY PAIN RELIEF PATCH- menthol 5% patch
- NDC Code(s): 0363-9950-05
- Packager: Walgreens Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 18, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
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Warnings
For external use only
When using this product
- use only as directed
- rare cases of serious burns have been reported with products of this type
- do not bandage tightly or use with heating pad or device
- avoid contact with the eyes or on mucous membranes
- do not apply to wounds or damaged skin
- do not use at the same time as other topical analgesics
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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 Ingredients
aloe vera extract, arnica montana extract, boswellia carterii resin extract, carboxymethylcellulose sodium, dihydroxyaluminum aminoacetate, ethylhexylglycerin, glycerin, green tea extract, iodopropynyl butylcarbamate, kaolin, mineral oil, petrolatum, phenoxyethanol, polyacrylic acid, polysorbate 80, povidone, propylene glycol, sodium polyacrylate, tartaric acid, titanium dioxide, water
- Questions or Comments
- Walgreens Cold Therapy Pain Relief Patch 5S
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INGREDIENTS AND APPEARANCE
WALGREENS COLD THERAPY PAIN RELIEF PATCH
menthol 5% patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-9950 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 GREEN TEA LEAF (UNII: W2ZU1RY8B0) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) MINERAL OIL (UNII: T5L8T28FGP) POLYACRYLIC ACID (450000 MW) (UNII: KD3S7H73D3) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) GLYCERIN (UNII: PDC6A3C0OX) POVIDONE (UNII: FZ989GH94E) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FRANKINCENSE (UNII: R9XLF1R1WM) PETROLATUM (UNII: 4T6H12BN9U) TARTARIC ACID (UNII: W4888I119H) WATER (UNII: 059QF0KO0R) DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) PHENOXYETHANOL (UNII: HIE492ZZ3T) CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) KAOLIN (UNII: 24H4NWX5CO) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J) POLYSORBATE 80 (UNII: 6OZP39ZG8H) ALOE VERA LEAF (UNII: ZY81Z83H0X) Product Characteristics Color Score Shape RECTANGLE Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-9950-05 5 in 1 CARTON 08/01/2022 1 9 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 08/01/2022 Labeler - Walgreens Company (008965063) Establishment Name Address ID/FEI Business Operations Foshan Aqua Gel Biotech Co., Ltd., 529128763 manufacture(0363-9950)