Label: ALCOHOL PREP PAD- isopropyl alcohol swab
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Contains inactivated NDC Code(s)
NDC Code(s): 35418-203-01, 35418-203-02, 35418-203-03 - Packager: ZEE MEDICAL
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 January 16, 2013
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- SPL UNCLASSIFIED SECTION
- Active ingredient
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- Inactive ingredient
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 100 Wipe Carton
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INGREDIENTS AND APPEARANCE
ALCOHOL PREP PAD
isopropyl alcohol swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:35418-203 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:35418-203-02 100 in 1 BOX 1 1 mL in 1 POUCH 2 NDC:35418-203-03 10 in 1 BOX 2 1 mL in 1 POUCH 3 NDC:35418-203-01 50 in 1 BOX 3 1 mL in 1 POUCH Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part344 01/15/2013 Labeler - ZEE MEDICAL (009645623) Registrant - DUKAL Corporation (791014871)