NDC 53462-007 Skin Antisepsis, Oral Cleansing, Nasal Antisepsis
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 53462-007?
What are the uses for Skin Antisepsis, Oral Cleansing, Nasal Antisepsis?
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)
- ALCOHOL (UNII: 3K9958V90M)
- GLYCERIN (UNII: PDC6A3C0OX)
- PEG-40 SORBITAN DIISOSTEARATE (UNII: JL4CCU7I1G)
- SACCHARIN SODIUM DIHYDRATE (UNII: SB8ZUX40TY)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- NONOXYNOL-9 (UNII: 48Q180SH9T)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- DIMETHICONE 350 (UNII: 2Y53S6ATLU)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- 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: 834127 - chlorhexidine gluconate 0.12 % Oral Rinse
- RxCUI: 834127 - chlorhexidine gluconate 1.2 MG/ML Mouthwash
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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".