NDC 59426-001 Provodine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 59426-001?
What are the uses for Provodine?
Which are Provodine UNII Codes?
The UNII codes for the active ingredients in this product are:
- POVIDONE-IODINE (UNII: 85H0HZU99M)
- IODINE (UNII: 9679TC07X4) (Active Moiety)
Which are Provodine 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:
- ALLANTOIN (UNII: 344S277G0Z)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
- GLYCERYL LAURATE (UNII: Y98611C087)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- LAURETH-7 (UNII: Z95S6G8201)
- NONOXYNOL-9 (UNII: 48Q180SH9T)
- OCTOXYNOL-9 (UNII: 7JPC6Y25QS)
- PIDOLIC ACID (UNII: SZB83O1W42)
- PEG-100 STEARATE (UNII: YD01N1999R)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y)
- WATER (UNII: 059QF0KO0R)
- BETASIZOFIRAN (UNII: 2X51AD1X3T)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TROLAMINE (UNII: 9O3K93S3TK)
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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".