Label: WALGREENS- ethyl alcohol gel
- NDC Code(s): 0363-0859-02, 0363-0859-08
- Packager: Walgreens
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 8, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- WARNINGS
- DOSAGE & ADMINISTRATION
- INDICATIONS & USAGE
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
WALGREENS
ethyl alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0859 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 700 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PEG-6 ISOSTEARATE (UNII: 0E2639OTJY) ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA) GLYCERIN (UNII: PDC6A3C0OX) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) ALOE VERA LEAF (UNII: ZY81Z83H0X) BASIC BLUE 1 (UNII: 92N74OA24D) FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF) ISOPROPYL ALCOHOL (UNII: ND2M416302) BASIC YELLOW 5 (UNII: 07BP340B4T) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0859-02 59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/15/2023 2 NDC:0363-0859-08 236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/15/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 02/15/2023 Labeler - Walgreens (008965063) Registrant - Apollo Health and Beauty Care Inc (201901209) Establishment Name Address ID/FEI Business Operations Apollo Health and Beauty Care Inc 201901209 manufacture(0363-0859)