Label: POVIDONE-IODINE PREP SWABSTICKS- povidone-iodine solution
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Contains inactivated NDC Code(s)
NDC Code(s): 50730-4102-3 - Packager: Triad Group
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated March 22, 2010
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- USES
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WARNINGS
For external use only.
Do not
- use in the eyes
- apply over large areas of the body
- use on individuals who are allergic or sensitive to iodine
- use as a first aid antiseptic for longer than 1 week unless directed by a doctor
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DIRECTIONS
For preparation of the skin prior to surgery
- clean the affected area
- remove swab by stick
- apply to the operative site prior to surgery
- clean the affected area
- apply a small amount of this product to the area 1-3 times daily
- may be covered with a sterile bandage
- if bandaged, let dry first
- SPL UNCLASSIFIED SECTION
- OTHER INFORMATION
- INACTIVE INGREDIENTS
- QUESTIONS
- POUCH INFORMATION
- CARTON INFORMATION
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INGREDIENTS AND APPEARANCE
POVIDONE-IODINE PREP SWABSTICKS
povidone-iodine solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50730-4102 Route of Administration TOPICAL, EPIDURAL, PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength povidone-iodine (UNII: 85H0HZU99M) (povidone-iodine - UNII:85H0HZU99M) povidone-iodine 0.10 mg in 1 mL Inactive Ingredients Ingredient Name Strength citric acid monohydrate (UNII: 2968PHW8QP) glycerin (UNII: PDC6A3C0OX) sodium hydroxide (UNII: 55X04QC32I) water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50730-4102-3 25 in 1 BOX 1 3 in 1 POUCH 1 1.7 mL in 1 APPLICATOR Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333 06/21/1985 Labeler - Triad Group (050259597) Establishment Name Address ID/FEI Business Operations Triad Group 050259597 manufacture