Label: ALCOHOL liquid
- NDC Code(s): 79481-0826-1, 79481-0826-3, 79481-0826-4
- Packager: Meijer
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 21, 2024
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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
ALCOHOL
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79481-0826 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 CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) GLYCERIN (UNII: PDC6A3C0OX) TOCOPHEROL (UNII: R0ZB2556P8) WATER (UNII: 059QF0KO0R) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) ALOE (UNII: V5VD430YW9) 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:79481-0826-3 236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/14/2021 2 NDC:79481-0826-1 59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/14/2021 3 NDC:79481-0826-4 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/14/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 01/14/2021 Labeler - Meijer (006959555) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091520 manufacture(79481-0826) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(79481-0826)