NDC 41163-052 Povidone Iodine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 41163 - Supervalu Inc
- 41163-052 - Povidone Iodine
Product Packages
NDC Code 41163-052-55
Package Description: 236 mL in 1 BOTTLE
Product Details
What is NDC 41163-052?
What are the uses for Povidone Iodine?
Which are Povidone Iodine UNII Codes?
The UNII codes for the active ingredients in this product are:
- POVIDONE-IODINE (UNII: 85H0HZU99M)
- POVIDONE-IODINE (UNII: 85H0HZU99M) (Active Moiety)
Which are Povidone Iodine Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Povidone Iodine?
- RxCUI: 312564 - povidone-iodine 10 % Topical Solution
- RxCUI: 312564 - povidone-iodine 100 MG/ML Topical Solution
- RxCUI: 312564 - povidone-iodine 10 % (titratable iodine 1 % ) Topical Solution
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".