Label: EQUATE MENTHOL PAIN RELIEVING- menthol patch
- NDC Code(s): 49035-870-01
- 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
- 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
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Inactive ingredients
carboxymethylcellulose sodium, dihydroxyaluminum aminoacetate, edetate disodium, ethylhexyl acrylate, glycerin, isopropyl myristate, partially neutralized polyacrylate, polyacrylic acid, polymethyl acrylate, polysorbate 80, polyvinyl alcohol, purified water, sodium polyacrylate starch, sorbeth-60 tetraoleate, sorbitan sesquioleate, sorbitol solution, talc, tartaric acid
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INGREDIENTS AND APPEARANCE
EQUATE MENTHOL PAIN RELIEVING
menthol patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-870 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM 50 mg Inactive Ingredients Ingredient Name Strength DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6) EDETATE DISODIUM (UNII: 7FLD91C86K) 2-ETHYLHEXYL ACRYLATE (UNII: HR49R9S6XG) GLYCERIN (UNII: PDC6A3C0OX) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) METHYL ACRYLATE (UNII: WC487PR91H) POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W) POLYSORBATE 80 (UNII: 6OZP39ZG8H) POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) WATER (UNII: 059QF0KO0R) SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) SORBITOL (UNII: 506T60A25R) TALC (UNII: 7SEV7J4R1U) TARTARIC ACID (UNII: W4888I119H) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49035-870-01 1 in 1 POUCH; Type 0: Not a Combination Product 01/01/2018 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)