Label: ADVANCED HAND SANITIZER- ethyl alcohol gel
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NDC Code(s):
59779-070-16,
59779-070-26,
59779-070-34,
59779-070-45, view more59779-070-49
- Packager: CVS Pharmacy, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 11, 2023
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
- Directions
- Other information
- Inactive ingredients
- Disclaimer
- Adverse reaction
- Principal display panel
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INGREDIENTS AND APPEARANCE
ADVANCED HAND SANITIZER
ethyl alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-070 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N) GLYCERIN (UNII: PDC6A3C0OX) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V) SULISOBENZONE (UNII: 1W6L629B4K) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59779-070-16 59 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 10/18/2013 2 NDC:59779-070-26 118 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 10/18/2013 3 NDC:59779-070-34 236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 10/18/2013 4 NDC:59779-070-49 443 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 10/18/2013 5 NDC:59779-070-45 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/18/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 10/18/2013 Labeler - CVS Pharmacy, Inc (062312574) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(59779-070) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(59779-070)