NDC 24909-201 Femmesil Creme Maximum Strength
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 24909 - Aidance Skincare & Topical Solutions, Llc
- 24909-201 - Femmesil Creme
Product Packages
NDC Code 24909-201-28
Package Description: 1 BOTTLE in 1 CARTON / 28 g in 1 BOTTLE
Product Details
What is NDC 24909-201?
What are the uses for Femmesil Creme Maximum Strength?
Which are Femmesil Creme Maximum Strength UNII Codes?
The UNII codes for the active ingredients in this product are:
- MICONAZOLE NITRATE (UNII: VW4H1CYW1K)
- MICONAZOLE (UNII: 7NNO0D7S5M) (Active Moiety)
Which are Femmesil Creme Maximum Strength 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:
- BENTONITE (UNII: A3N5ZCN45C)
- JOJOBA OIL (UNII: 724GKU717M)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- SILVER OXIDE (UNII: 897WUN6G6T)
- TEA TREE OIL (UNII: VIF565UC2G)
- WATER (UNII: 059QF0KO0R)
- ZINC OXIDE (UNII: SOI2LOH54Z)
What is the NDC to RxNorm Crosswalk for Femmesil Creme Maximum Strength?
- RxCUI: 1250729 - Femmesil 2 % Topical Cream
- RxCUI: 1250729 - miconazole nitrate 20 MG/ML Topical Cream [Femmesil]
- RxCUI: 1250729 - Femmesil 20 MG/ML Topical Cream
- RxCUI: 998483 - miconazole nitrate 2 % Topical Cream
- RxCUI: 998483 - miconazole nitrate 20 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".