NDC 53462-008 Skin Antisepsis, Oral Cleansing, Nasal Antisepsis
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 53462-008?
Which are Skin Antisepsis, Oral Cleansing, Nasal Antisepsis UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)
- CHLORHEXIDINE (UNII: R4KO0DY52L) (Active Moiety)
- POVIDONE-IODINE (UNII: 85H0HZU99M)
- IODINE (UNII: 9679TC07X4) (Active Moiety)
Which are Skin Antisepsis, Oral Cleansing, Nasal Antisepsis 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:
- WATER (UNII: 059QF0KO0R)
- NONOXYNOL-9 (UNII: 48Q180SH9T)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- DIMETHICONE 350 (UNII: 2Y53S6ATLU)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLUCONOLACTONE (UNII: WQ29KQ9POT)
- LACTIC ACID (UNII: 33X04XA5AT)
- LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)
- MALIC ACID (UNII: 817L1N4CKP)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- SODIUM IODIDE (UNII: F5WR8N145C)
- PEG-100 STEARATE (UNII: YD01N1999R)
- XYLITOL (UNII: VCQ006KQ1E)
What is the NDC to RxNorm Crosswalk for Skin Antisepsis, Oral Cleansing, Nasal Antisepsis?
- RxCUI: 252965 - povidone-iodine 5 % Topical Solution
- RxCUI: 252965 - povidone-iodine 50 MG/ML Topical Solution
- RxCUI: 252965 - povidone-iodine 5 % (titratable iodine 0.5 % ) Topical Solution
- RxCUI: 846127 - chlorhexidine gluconate 2 % Medicated Pad
- RxCUI: 846127 - chlorhexidine gluconate 20 MG/ML Medicated Pad
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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".