Label: PAIN RELIEVING PATCHES- camphor menthol methyl salicytate patch
- NDC Code(s): 0363-9903-40
- Packager: Walgreen Company
- 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.
Drug Label Information
Updated January 11, 2023
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENThydrogenated poly, pentaerythrityl tetra-di-t-butyl hydroxyhydrocinnamate, petroleum, styrene/isoprene copolymer
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PURPOSE
- When using this product:
- Do not use
- top use and consult a doctor
- Storage and Care
- Pain Relieving Path
-
INGREDIENTS AND APPEARANCE
PAIN RELIEVING PATCHES
camphor menthol methyl salicytate patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-9903 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) 1.2 g in 100 g MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 5.7 g in 100 g METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 6.3 g in 100 g Inactive Ingredients Ingredient Name Strength HYDROGENATED POLY(C6-14 OLEFIN; 2 CST) (UNII: P0TX083987) PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS) LIQUID PETROLEUM (UNII: 6ZAE7X688J) STYRENE (UNII: 44LJ2U959V) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-9903-40 40 in 1 BOX 11/15/2019 1 9 g in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 11/15/2019 Labeler - Walgreen Company (008965063) Establishment Name Address ID/FEI Business Operations Foshan Aqua Gel Biotech Co.,Ltd. 529128763 manufacture(0363-9903)