Label: ANTIBACTERIAL HAND SANITIZER- alcohol liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 77879-002-01, 77879-002-02 - Packager: BT Supplies West Inc
- 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 February 9, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Uses
- Warnings
- Directions
- Other information
- Inactive ingredients
- Package Labeling: 473ml
- 77879-002-02 3.8L Label
-
INGREDIENTS AND APPEARANCE
ANTIBACTERIAL HAND SANITIZER
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:77879-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.73 mL in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) SQUALANE (UNII: GW89575KF9) PANTHENOL (UNII: WV9CM0O67Z) INULIN (UNII: JOS53KRJ01) HYALURONATE SODIUM (UNII: YSE9PPT4TH) FRUCTOSE (UNII: 6YSS42VSEV) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:77879-002-01 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/27/2020 2 NDC:77879-002-02 3800 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/27/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 05/27/2020 Labeler - BT Supplies West Inc (033878488)