Label: EQUATE PAIN RELIEF PATCH CAMPHOR/MENTHOL/SALICYLATE- camphor, menthol, methyl salicylate patch
- NDC Code(s): 79903-039-60
- Packager: Walmart Stores Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 18, 2024
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
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Warnings
For external use only
Allergy alert:
If prone to allergic reaction from aspirin or salicylates, consult a doctor before use.
Do not use
- on wounds or damaged skin
- with a heating pad
- if you are allergic to any ingredients of this product
- Do not use otherwise than as directed
When using this product
- use only as directed
- avoid contact with the eyes, mucous membranes, or rashes
- do not bandage tightly
- Do not use at the same time as other topical analgesics
- Dispose of used patch away from children and pets. Used patches still contain the drug product that can produce serious adverse effects if a child or pet chews or ingests this patch.
- Directions
- Other information
- Inactive ingredients
- Equate Pain Relief Patch Camphor/Menthol/Salicylate
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INGREDIENTS AND APPEARANCE
EQUATE PAIN RELIEF PATCH CAMPHOR/MENTHOL/SALICYLATE
camphor, menthol, methyl salicylate patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79903-039 Route of Administration PERCUTANEOUS, TOPICAL, TRANSDERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) 3.1 g in 100 g MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 6 g in 100 g METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 10 g in 100 g Inactive Ingredients Ingredient Name Strength LIQUID PETROLEUM (UNII: 6ZAE7X688J) PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS) STYRENE/ACRYLAMIDE COPOLYMER (MW 500000) (UNII: 5Z4DPO246A) HYDROGENATED POLYDECENE TYPE I (UNII: U333RI6EB7) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79903-039-60 60 in 1 BOX 01/01/2021 1 6 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 Drug M017 01/01/2021 Labeler - Walmart Stores Inc (051957769) Establishment Name Address ID/FEI Business Operations Foshan Aqua Gel Biotech Co., Ltd., 529128763 manufacture(79903-039)