Label: DR. WONJIN HAND SAFER SANIGEL- ethanol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 75708-7502-2 - Packager: BEAUTY SKIN.CO.,Ltd.
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated May 9, 2020
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INGREDIENTS AND APPEARANCE
DR. WONJIN HAND SAFER SANIGEL
ethanol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75708-7502 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 1.5 mL in 2 mL Inactive Ingredients Ingredient Name Strength LEMON (UNII: 24RS0A988O) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) ALOE VERA LEAF (UNII: ZY81Z83H0X) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) WATER (UNII: 059QF0KO0R) TROLAMINE (UNII: 9O3K93S3TK) CENTELLA ASIATICA (UNII: 7M867G6T1U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75708-7502-2 50 in 1 BOX 05/10/2020 1 2 mL 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 part333A 05/10/2020 Labeler - BEAUTY SKIN.CO.,Ltd. (688530942) Establishment Name Address ID/FEI Business Operations BEAUTY SKIN.CO.,Ltd. 688530942 manufacture(75708-7502)