Label: INSTANT HAND SANITIZER liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 55447-001-01 - Packager: Nan tong Feilong Natural Healthy 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 13, 2020
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- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- INDICATIONS & USAGE
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- PURPOSE
- WARNINGS
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INGREDIENTS AND APPEARANCE
INSTANT HAND SANITIZER
instant hand sanitizer liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55447-001 Route of Administration EXTRACORPOREAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 375 mL in 500 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) ISOPROPYL ALCOHOL (UNII: ND2M416302) WATER (UNII: 059QF0KO0R) 2-(2-ETHYLHEXYLOXY)ETHANOL (UNII: 04CQ74YVIS) Product Characteristics Color Score Shape Size Flavor Imprint Code drmagic Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55447-001-01 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/13/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 04/13/2020 Labeler - Nan tong Feilong Natural Healthy Co.,LTD (554529828) Establishment Name Address ID/FEI Business Operations Nan tong Feilong Natural Healthy Co.,LTD 554529828 manufacture(55447-001)