NDC 53943-994 Tolnaftate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53943 - Discount Drug Mart, Inc.
- 53943-994 - Tolnaftate
Product Packages
NDC Code 53943-994-01
Package Description: 1 TUBE in 1 BOX / 28.3 g in 1 TUBE
Product Details
What is NDC 53943-994?
What are the uses for Tolnaftate?
Which are Tolnaftate UNII Codes?
The UNII codes for the active ingredients in this product are:
- TOLNAFTATE (UNII: 06KB629TKV)
- TOLNAFTATE (UNII: 06KB629TKV) (Active Moiety)
Which are Tolnaftate 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:
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PARAFFIN (UNII: I9O0E3H2ZE)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- WATER (UNII: 059QF0KO0R)
- CHLOROCRESOL (UNII: 36W53O7109)
- SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
- MYRISTOYL/PALMITOYL OXOSTEARAMIDE/ARACHAMIDE MEA (UNII: 1211AIM8G7)
What is the NDC to RxNorm Crosswalk for Tolnaftate?
- RxCUI: 103951 - tolnaftate 1 % Topical Cream
- RxCUI: 103951 - tolnaftate 10 MG/ML Topical Cream
* Please review the disclaimer below.
Patient Education
Tolnaftate
Tolnaftate stops the growth of fungi that cause skin infections, including athlete's foot, jock itch, and ringworm. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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* Please review the disclaimer below.
[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".