NDC 59779-295 Itch Relief Clear Skin Protectant Cvs
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 59779-295?
What are the uses for Itch Relief Clear Skin Protectant Cvs?
Which are Itch Relief Clear Skin Protectant Cvs UNII Codes?
The UNII codes for the active ingredients in this product are:
- PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5)
- PRAMOXINE (UNII: 068X84E056) (Active Moiety)
- ZINC ACETATE (UNII: FM5526K07A)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Itch Relief Clear Skin Protectant Cvs 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:
- ALCOHOL (UNII: 3K9958V90M)
- OATMEAL (UNII: 8PI54V663Y)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POLYSORBATE 40 (UNII: STI11B5A2X)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Itch Relief Clear Skin Protectant Cvs?
- RxCUI: 1294033 - pramoxine HCl 1 % / zinc acetate 0.1 % Topical Spray
- RxCUI: 1294033 - pramoxine hydrochloride 10 MG/ML / zinc acetate 1 MG/ML Topical Spray
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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".