Label: POVIDINE IODINE swab
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Contains inactivated NDC Code(s)
NDC Code(s): 0404-5637-01 - Packager: Henry Schein Inc
- 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 May 9, 2011
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- Uses: PVP Prep Pad
- Warnings:
- Do not use:
- Ask a doctor before use if you have:
- Stop Use:
- Keep Out Of Reach Of Children
- Directions:
- Inactive Ingredient:
- INDICATIONS & USAGE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
POVIDINE IODINE
povidine iodine swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0404-5637 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POVIDONE-IODINE (UNII: 85H0HZU99M) (POVIDONE-IODINE - UNII:85H0HZU99M) POVIDONE-IODINE 10 mL in 100 mL Inactive Ingredients Ingredient Name Strength NONOXYNOL-9 (UNII: 48Q180SH9T) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0404-5637-01 10 in 1 CASE 1 100 in 1 BOX 1 .3 mL in 1 POUCH Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333C 03/17/2011 Labeler - Henry Schein Inc (012430880)