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
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated May 9, 2020
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- PRINCIPAL DISPLAY PANEL
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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)
