Label: POVIDONE-IODINE PREP- povidone-iodine patch
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Contains inactivated NDC Code(s)
NDC Code(s): 44019-100-00 - Packager: Yinjing Medical Technology (Shanghai) Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 December 28, 2017
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Uses
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Warnings
- For external use only
Do not use
- in the eyes or apply over large areas of the body
- longer than 1 week unless directed by a doctor
- on individuals who are sensitive or allergic to iodine
- Directions
- Inactive ingredient
- Other information
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
POVIDONE-IODINE PREP
povidone-iodine patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:44019-100 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE 10 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:44019-100-00 1 in 1 POUCH 07/07/2017 1 0.45 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.) Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 07/07/2017 Labeler - Yinjing Medical Technology (Shanghai) Co., Ltd. (530501535)