Label: POVIDONE IODINE swab
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Contains inactivated NDC Code(s)
NDC Code(s): 68183-116-01 - Packager: Custom Kits Company Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated January 17, 2020
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient
- Purpose
- Directions
- Warnings
- Ask a Doctor before use if you have
- Stop Use
- Keep Out Of Reach Of Children
- Directions
- Other Information
- Inactive Ingredient
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
POVIDONE IODINE
povidone iodine swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68183-116 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE 10 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68183-116-01 10 mL in 1 BOX, UNIT-DOSE; Type 0: Not a Combination Product 10/14/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/14/2015 Labeler - Custom Kits Company Inc (928643712) Establishment Name Address ID/FEI Business Operations James Alexander Corporation 040756421 manufacture(68183-116) Establishment Name Address ID/FEI Business Operations Custom Kits Company Inc 928643712 repack(68183-116) , relabel(68183-116)