Label: ALCOHOL PREP- isopropyl alcohol swab
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Contains inactivated NDC Code(s)
NDC Code(s): 0924-0011-06 - Packager: Acme United Corporation
- Category: HUMAN OTC DRUG LABEL
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 July 8, 2014
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- Purpose
- Warnings:
- Indications and Usage:
- Keep out of reach of children.
- Directions:
- Other information:
- Inactive Ingredient
- Principal Display Panel - box
- Principal Display Panel - packet
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INGREDIENTS AND APPEARANCE
ALCOHOL PREP
isopropyl alcohol swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0924-0011 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 0.7 mL in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0924-0011-06 100 in 1 BOX 1 0.55 mL in 1 PACKET Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 07/08/2014 Labeler - Acme United Corporation (001180207) Registrant - Dynarex Corporation (008124539)