Label: POVIDINE IODINE swab
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Contains inactivated NDC Code(s)
NDC Code(s): 67777-301-01, 67777-301-02 - Packager: Dynarex Corporation
- 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 February 10, 2012
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- Uses:
- Warnings:
- Do not use:
- Ask a doctor before use if you have:
- Stop Use:
- Keep Out Of Reach Of Children
- Directions Povidone Iodine Gel Swabstick:
- Other information:
- INDICATIONS & USAGE
- Inactive Ingredients
- 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:67777-301 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-10 (UNII: K7O76887AP) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67777-301-01 10 in 1 CASE 1 50 in 1 BOX 1 1 in 1 POUCH 1 .3 mL in 1 POUCH 2 NDC:67777-301-02 10 in 1 CASE 2 25 in 1 BOX 2 3 in 1 POUCH 2 .9 mL in 1 POUCH Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333C 02/10/2012 Labeler - Dynarex Corporation (008124539) Registrant - Dynarex Corporation (008124539)