Label: ALCOHOL PREP PAD liquid
- NDC Code(s): 51142-444-01
- Packager: ASO LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated November 10, 2022
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings
- Do not use
- Stop use if
- Keep out of reach of children
- Directions
- Other Information
- Inactice ingredient
- Principal DIsplay Panel
-
INGREDIENTS AND APPEARANCE
ALCOHOL PREP PAD
alcohol prep pad liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51142-444 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Product Characteristics Color white (white pad) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51142-444-01 0.4 mL in 1 POUCH; Type 0: Not a Combination Product 09/24/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 09/24/2018 Labeler - ASO LLC (152793493)