- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
glycol salicylate, dl-camphor, gardenia fruit soft extract, xanthoxylum fruit 30% ethanol soft extract, tocopherol acetate, glycyrrhizic acid, polysorbate 80, sorbitan sesquioleate, carboxymethylcellulose sodium, sodium polyacrylate, kaolin, dried aluminium hydroxide gel, disodium edetate hydrate, concentrated glycerin, gelatin, nikazole ts-620, methylparaben, propylparaben, tartaric acid , purified water, nonwoven fabric, polypropylene film
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
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INDICATIONS & USAGE
step 1: remove the colored protective sheet from the adhesive tape strip
step 2: attach the cotton side of Zenol medicated patch to the adhesive tape
step 3: remove the transparent protective film from the patch, and also the remainder of the colored protective sheet (the two strips with arrows on the side)
step 4: apply one or twice daily or as needed, to the affected skin surface
step 5: following the use, tightly close and fold the open end of the pack, in order to preserve the efficacy of the remaining patch - WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HANBANG CATAPLASMA
menthol poulticeProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61476-102 Route of Administration TRANSDERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM 280 mg in 12 g Inactive Ingredients Ingredient Name Strength GLYCOL SALICYLATE (UNII: 3I1VBB7AXH) CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) GELATIN, UNSPECIFIED (UNII: 2G86QN327L) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61476-102-01 12 g in 1 PATCH; Type 0: Not a Combination Product 12/03/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 12/03/2013 11/10/2023 Labeler - Green Cross Corp (687760561) Establishment Name Address ID/FEI Business Operations Green Cross Corp 689852033 manufacture(61476-102)