Label: ALCOHOL liquid
- NDC Code(s): 11344-849-16, 11344-849-34, 11344-849-45
- Packager: Consumer Product Partners, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 1, 2024
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- Official Label (Printer Friendly)
- Claims
- 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
- Claims
- SPL UNCLASSIFIED SECTION
- Principal panel display
-
INGREDIENTS AND APPEARANCE
ALCOHOL
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11344-849 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 WATER (UNII: 059QF0KO0R) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) GLYCERIN (UNII: PDC6A3C0OX) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) TOCOPHEROL (UNII: R0ZB2556P8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11344-849-16 59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/29/2020 2 NDC:11344-849-34 236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/29/2020 3 NDC:11344-849-45 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/29/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 04/29/2020 Labeler - Consumer Product Partners, LLC (119091520) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091520 manufacture(11344-849) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(11344-849)