NDC 52261-0100 Forticept Antifungal Balm
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52261 - Cosco International, Inc.
- 52261-0100 - Forticept Antifungal Balm
Product Packages
NDC Code 52261-0100-0
Package Description: 30 g in 1 TUBE
NDC Code 52261-0100-1
Package Description: 60 g in 1 TUBE
Product Details
What is NDC 52261-0100?
What are the uses for Forticept Antifungal Balm?
Which are Forticept Antifungal Balm UNII Codes?
The UNII codes for the active ingredients in this product are:
- TOLNAFTATE (UNII: 06KB629TKV)
- TOLNAFTATE (UNII: 06KB629TKV) (Active Moiety)
Which are Forticept Antifungal Balm 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)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIHEPTYL SUCCINATE (UNII: 057N7SS26Y)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- GLYCERYL DIBEHENATE (UNII: R8WTH25YS2)
- PEG-40 CASTOR OIL (UNII: 4ERD2076EF)
- POLYGLYCERYL-10 OLEATE (UNII: 55C81W76DH)
- POLIHEXANIDE HYDROCHLORIDE (UNII: 4XI6112496)
- METHYL LACTATE, (-)- (UNII: 0379G9C44S)
- TEA TREE OIL (UNII: VIF565UC2G)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- GLYCERYL CAPRATE (UNII: 197M6VFC1W)
- ACACIA DECURRENS FLOWER (UNII: 8PHF3LSM61)
What is the NDC to RxNorm Crosswalk for Forticept Antifungal Balm?
- RxCUI: 313423 - tolnaftate 1 % Topical Solution
- RxCUI: 313423 - tolnaftate 10 MG/ML Topical Solution
* 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".