NDC 43128-035 Pro Advantage Fast Absorbing Perineal With Dimethicone Skin Protectant
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 43128-035?
What are the uses for Pro Advantage Fast Absorbing Perineal With Dimethicone Skin Protectant?
Which are Pro Advantage Fast Absorbing Perineal With Dimethicone Skin Protectant UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Pro Advantage Fast Absorbing Perineal With Dimethicone Skin Protectant 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)
- MINERAL OIL (UNII: T5L8T28FGP)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- TROLAMINE (UNII: 9O3K93S3TK)
- ALLANTOIN (UNII: 344S277G0Z)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
What is the NDC to RxNorm Crosswalk for Pro Advantage Fast Absorbing Perineal With Dimethicone Skin Protectant?
- RxCUI: 244642 - dimethicone 2 % Topical Cream
- RxCUI: 244642 - dimethicone 20 MG/ML Topical Cream
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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".