Label: HAND SANITIZER 1.85OZ- alcohol gel
- NDC Code(s): 52000-131-01
- Packager: UNIVERSAL DISTRIBUTION CENTER LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 1, 2023
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- Active ingredient
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- WARNINGS
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
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- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HAND SANITIZER 1.85OZ
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52000-131 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62 mL in 100 mL Inactive Ingredients Ingredient Name Strength FD&C RED NO. 40 (UNII: WZB9127XOA) WATER (UNII: 059QF0KO0R) CARBOMER 934 (UNII: Z135WT9208) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) ALOE VERA LEAF (UNII: ZY81Z83H0X) D&C RED NO. 33 (UNII: 9DBA0SBB0L) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52000-131-01 54.7 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/01/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 01/01/2018 Labeler - UNIVERSAL DISTRIBUTION CENTER LLC (019180459) Registrant - UNIVERSAL DISTRIBUTION CENTER LLC (019180459)