NDC 54868-5351 Derma-smoothe/fs
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5351 - Derma-smoothe/fs
Product Packages
NDC Code 54868-5351-0
Package Description: 1 BOTTLE in 1 CARTON / 118.28 mL in 1 BOTTLE
Product Details
What is NDC 54868-5351?
What are the uses for Derma-smoothe/fs?
Which are Derma-smoothe/fs UNII Codes?
The UNII codes for the active ingredients in this product are:
- FLUOCINOLONE ACETONIDE (UNII: 0CD5FD6S2M)
- FLUOCINOLONE ACETONIDE (UNII: 0CD5FD6S2M) (Active Moiety)
Which are Derma-smoothe/fs 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:
- PEANUT OIL (UNII: 5TL50QU0W4)
- LIGHT MINERAL OIL (UNII: N6K5787QVP)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- OLETH-2 (UNII: 7L6R1SQ6M0)
What is the NDC to RxNorm Crosswalk for Derma-smoothe/fs?
- RxCUI: 1191307 - fluocinolone acetonide 0.01 % Topical Oil
- RxCUI: 1191307 - fluocinolone acetonide 0.1 MG/ML Topical Oil
- RxCUI: 1191307 - fluocinolone acetonide 0.011 % Topical Oil
- RxCUI: 1191309 - Derma-Smoothe/FS Scalp 0.01 % Topical Oil
- RxCUI: 1191309 - fluocinolone acetonide 0.1 MG/ML Topical Oil [Derma-Smoothe FS]
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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".