Label: ALCOHOL PREP- isopropyl alcohol swab
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NDC Code(s):
67777-121-11,
67777-121-12,
67777-121-13,
67777-121-14, view more67777-121-16, 67777-121-17, 67777-121-18, 67777-121-19, 67777-121-20, 67777-121-21, 67777-121-22, 67777-121-23, 67777-121-24, 67777-121-26, 67777-121-27
- Packager: Dynarex Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 12, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use(s)
- Warnings
- Directions
- Other Information
- Inactive Ingredient
- Label
- Label 1113-50
- Label 1113UB-24
- Label 1113UB-10
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INGREDIENTS AND APPEARANCE
ALCOHOL PREP
isopropyl alcohol swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67777-121 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) Product Characteristics Color Score Shape RECTANGLE Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67777-121-20 20000 in 1 CASE 07/01/2010 1 NDC:67777-121-19 100 in 1 BOX 1 NDC:67777-121-14 0.55 mL in 1 POUCH; Type 0: Not a Combination Product 2 NDC:67777-121-18 1000 in 1 CASE 07/01/2010 2 NDC:67777-121-17 100 in 1 BOX 2 NDC:67777-121-16 0.7 mL in 1 POUCH; Type 0: Not a Combination Product 3 NDC:67777-121-12 2000 in 1 CASE 07/01/2010 3 NDC:67777-121-11 200 in 1 BOX 3 NDC:67777-121-13 0.55 mL in 1 POUCH; Type 0: Not a Combination Product 4 NDC:67777-121-26 1000 in 1 CASE 07/01/2010 4 NDC:67777-121-27 50 in 1 BOX 4 0.55 mL in 1 POUCH; Type 0: Not a Combination Product 5 NDC:67777-121-22 480 in 1 CASE 07/01/2010 5 NDC:67777-121-21 24 in 1 BOX 5 0.55 mL in 1 POUCH; Type 0: Not a Combination Product 6 NDC:67777-121-24 1000 in 1 CASE 07/01/2010 6 NDC:67777-121-23 10 in 1 BOX 6 0.55 mL in 1 POUCH; 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 07/01/2010 Labeler - Dynarex Corporation (008124539)