Label: ALCOHOL PREP- isopropyl alcohol swab
- NDC Code(s): 76162-809-30
- Packager: Topco Associates
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 27, 2023
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
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Warnings
- For external use only.
- Flammable. Keep away from fire or flame.
When using this product
- do not get into eyes
- do not apply over large areas of the body
- in case of deep or puncture wounds, animal bites or serious burns, consult a doctor
- Directions
- Other information
- Inactive ingredients
- Manufacturing Information
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
ALCOHOL PREP
isopropyl alcohol swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76162-809 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) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76162-809-30 100 in 1 BOX 07/13/2011 12/31/2026 1 1 in 1 PACKET 1 0.5 mL in 1 APPLICATOR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 07/13/2011 12/31/2026 Labeler - Topco Associates (006935977)