NDC 36800-874 Clear Itch Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 36800 - Topcare
- 36800-874 - Clear Itch Relief
Product Packages
NDC Code 36800-874-03
Package Description: 85 g in 1 CAN
Product Details
What is NDC 36800-874?
What are the uses for Clear Itch Relief?
Which are Clear Itch Relief 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 Clear Itch Relief 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 Clear Itch Relief?
- 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".