Label: COMPANION HAND SANITIZER- hand sanitizer liquid
- NDC Code(s): 59051-7100-1, 59051-7100-2, 59051-7100-3
- Packager: Neogen Corporation
- 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 July 24, 2023
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- Official Label (Printer Friendly)
- DRUG FACTS Active ingredients
- PURPOSE
- USES
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
COMPANION HAND SANITIZER
hand sanitizer liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59051-7100 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 338.82 g in 1 L Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) PEG-10 ACRYLATE/PERFLUOROHEXYLETHYL ACRYLATE COPOLYMER (UNII: D76Z87928N) 2-(PERFLUOROHEXYL)ETHANOL (UNII: G2R5YO5N3V) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59051-7100-2 16 in 1 PACKAGE, COMBINATION 06/05/2017 1 NDC:59051-7100-1 0.2 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 2 NDC:59051-7100-3 3.78 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/05/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 06/05/2017 Labeler - Neogen Corporation (042125879) Registrant - Preserve International (117315289) Establishment Name Address ID/FEI Business Operations Preserve Inc. 808154199 manufacture(59051-7100) , api manufacture(59051-7100)