NDC 76348-417 Gold Mountain Beauty Fungal Nail Eliminator
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76348 - Renu Laboratories, Inc.
- 76348-417 - Gold Mountain Beauty Fungal Nail Eliminator
Product Packages
NDC Code 76348-417-02
Package Description: 1 BOTTLE, GLASS in 1 BOX / 14 g in 1 BOTTLE, GLASS (76348-417-01)
Product Details
What is NDC 76348-417?
What are the uses for Gold Mountain Beauty Fungal Nail Eliminator?
Which are Gold Mountain Beauty Fungal Nail Eliminator UNII Codes?
The UNII codes for the active ingredients in this product are:
- TOLNAFTATE (UNII: 06KB629TKV)
- TOLNAFTATE (UNII: 06KB629TKV) (Active Moiety)
Which are Gold Mountain Beauty Fungal Nail Eliminator 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:
- TEA TREE OIL (UNII: VIF565UC2G)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- TRIMETHYLPENTANEDIOL/ADIPIC ACID/GLYCERIN CROSSPOLYMER (25000 MPA.S) (UNII: 587WKM3S9Q)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- HIPPOPHAE RHAMNOIDES FRUIT OIL (UNII: TA4JCF9S1J)
- HIPPOPHAE RHAMNOIDES SEED OIL (UNII: T53SBG6741)
- DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
- THYME OIL (UNII: 2UK410MY6B)
- EVENING PRIMROSE OIL (UNII: 3Q9L08K71N)
- WINTER SAVORY OIL (UNII: EP61SM69Z2)
What is the NDC to RxNorm Crosswalk for Gold Mountain Beauty Fungal Nail Eliminator?
- RxCUI: 1362937 - tolnaftate 1 % Topical Oil
- RxCUI: 1362937 - tolnaftate 10 MG/ML Topical Oil
* 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".