Label: HAND SANITIZER USA liquid
HAND SANITIZER- alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 74010-3010-1, 74010-3010-2, 74010-3010-3, 74010-3010-4, view more74010-3010-5, 74010-3010-6, 74010-3016-1, 74010-3016-2, 74010-3016-3, 74010-3016-4, 74010-3016-5, 74010-3016-6 - Packager: Global Universal SRL LLC dba Minhas Micro Distillery
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Export only
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 7, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Hand Sanitizer EXPORT
- Hand Sanitizer USA
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INGREDIENTS AND APPEARANCE
HAND SANITIZER USA
hand sanitizer usa liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74010-3016 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 80 mL in 100 mL Inactive Ingredients Ingredient Name Strength DENATONIUM BENZOATE ANHYDROUS (UNII: M5BA6GAF1O) HYDROGEN PEROXIDE (UNII: BBX060AN9V) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) Product Characteristics Color white (clear liquid) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74010-3016-1 50 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/30/2020 2 NDC:74010-3016-2 200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/30/2020 3 NDC:74010-3016-5 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/30/2020 4 NDC:74010-3016-3 375 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/30/2020 5 NDC:74010-3016-6 1140 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/30/2020 6 NDC:74010-3016-4 750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/30/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/26/2020 HAND SANITIZER
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74010-3010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 80 mL in 100 mL Inactive Ingredients Ingredient Name Strength HYDROGEN PEROXIDE (UNII: BBX060AN9V) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) Product Characteristics Color white (clear liquid) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74010-3010-1 50 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/29/2020 2 NDC:74010-3010-2 200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/30/2020 3 NDC:74010-3010-4 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/30/2020 4 NDC:74010-3010-3 375 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/30/2020 5 NDC:74010-3010-5 1140 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/30/2020 6 NDC:74010-3010-6 750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/30/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Export only 03/26/2020 Labeler - Global Universal SRL LLC dba Minhas Micro Distillery (066395536) Establishment Name Address ID/FEI Business Operations Global Universal SRL LLC dba Minhas Micro Distillery 066395536 manufacture(74010-3016, 74010-3010) , repack(74010-3016, 74010-3010)