Label: DRS CLEAN HAND GEL- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 75193-0001-1 - Packager: EROOM FACTORY 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 April 12, 2020
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DRS CLEAN HAND GEL
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75193-0001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) HYALURONATE SODIUM (UNII: YSE9PPT4TH) CARBOMER 940 (UNII: 4Q93RCW27E) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75193-0001-1 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/01/2020 Labeler - EROOM FACTORY Co., Ltd. (694819890) Registrant - EROOM FACTORY Co., Ltd. (694819890) Establishment Name Address ID/FEI Business Operations EROOM FACTORY Co., Ltd. 694819890 manufacture(75193-0001)