NDC 65373-500 Tineacide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 65373-500?
What are the uses for Tineacide?
Which are Tineacide UNII Codes?
The UNII codes for the active ingredients in this product are:
- UNDECYLENIC ACID (UNII: K3D86KJ24N)
- UNDECYLENIC ACID (UNII: K3D86KJ24N) (Active Moiety)
Which are Tineacide 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)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CLOTRIMAZOLE (UNII: G07GZ97H65)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- HYDROXYETHYL CELLULOSE (140 CPS AT 5%) (UNII: 8136Y38GY5)
- ENGLISH LAVENDER OIL (UNII: ZBP1YXW0H8)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POLYOXYL 100 STEARATE (UNII: YD01N1999R)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TEA TREE OIL (UNII: VIF565UC2G)
- TROLAMINE (UNII: 9O3K93S3TK)
- UREA (UNII: 8W8T17847W)
What is the NDC to RxNorm Crosswalk for Tineacide?
- RxCUI: 1250976 - Tineacide Antifungal 10 % Topical Cream
- RxCUI: 1250976 - undecylenic acid 100 MG/ML Topical Cream [Tineacide Antifungal]
- RxCUI: 1250976 - Tineacide Antifungal 100 MG/ML Topical Cream
- RxCUI: 1250978 - undecylenic acid 13 % Topical Cream
- RxCUI: 1250978 - undecylenic acid 130 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".