Label: EQUATE CAPSAICIN PAIN RELIEVING- capsaicin patch
- NDC Code(s): 49035-890-01, 49035-890-04
- Packager: Wal-Mart Stores Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 17, 2024
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- Active ingredient
- Purpose
- Uses
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Warnings
For external use only
When using this product
- use only as directed
- do not use at least 1 hours before, or immediately after, a bath or shower
- avoid contact with eyes and mucous membranes
- do not apply to wounds or to damaged or very sensitive skin
- do not bandage tightly or use with a heating pad
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Directions
- adults and children 12 years and over: apply to affected area; change patch 1 to 2 times daily
- children under 12 years: ask a doctor
- FOR BEST RESULTS: apply to clean, dry skin
- tear open pouch and remove patch; if desired, cut patch to size
- grasp both ends of the patch firmly with thumbs near center
- stretch patch until the backing separates
- remove protective film while applying patch directly to site of pain
- WASH HANDS WITH SOAP AND WATER AFTER APPLYING
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Inactive ingredients
carboxymethylcellulose sodium, castor oil, dihydroxyaluminum aminoacetate, edetate disodium, glycerin, methylparaben, partially neutralized polyacrylate, polyacrylic acid, polysorbate 80, polyvinyl alcohol, propylene glycol monocaprylate, purified water, sodium polyacrylate, sodium polyacrylate starch, sorbitol solution, talc, tartaric acid
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INGREDIENTS AND APPEARANCE
EQUATE CAPSAICIN PAIN RELIEVING
capsaicin patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-890 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM) CAPSAICIN 0.25 mg in 1 g Inactive Ingredients Ingredient Name Strength CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) CASTOR OIL (UNII: D5340Y2I9G) DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6) EDETATE DISODIUM (UNII: 7FLD91C86K) GLYCERIN (UNII: PDC6A3C0OX) METHYLPARABEN (UNII: A2I8C7HI9T) POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W) POLYSORBATE 80 (UNII: 6OZP39ZG8H) POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) PROPYLENE GLYCOL CAPRYLATE (UNII: RT9P9S09QI) WATER (UNII: 059QF0KO0R) SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L) SORBITOL (UNII: 506T60A25R) TALC (UNII: 7SEV7J4R1U) TARTARIC ACID (UNII: W4888I119H) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49035-890-01 1 in 1 POUCH 01/01/2018 1 0.0035 g in 1 PATCH; Type 0: Not a Combination Product 2 NDC:49035-890-04 4 in 1 POUCH 01/01/2018 2 0.0035 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 01/01/2018 Labeler - Wal-Mart Stores Inc (051957769)
