NDC 54868-6307 Claravis
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 54868-6307?
What are the uses for Claravis?
Which are Claravis UNII Codes?
The UNII codes for the active ingredients in this product are:
- ISOTRETINOIN (UNII: EH28UP18IF)
- ISOTRETINOIN (UNII: EH28UP18IF) (Active Moiety)
Which are Claravis 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:
- BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GELATIN (UNII: 2G86QN327L)
- COTTONSEED OIL (UNII: H3E878020N)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- SOYBEAN OIL (UNII: 241ATL177A)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- WHITE WAX (UNII: 7G1J5DA97F)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- AMMONIA (UNII: 5138Q19F1X)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SHELLAC (UNII: 46N107B71O)
- DIMETHICONE (UNII: 92RU3N3Y1O)
What is the NDC to RxNorm Crosswalk for Claravis?
- RxCUI: 197844 - ISOtretinoin 20 MG Oral Capsule
- RxCUI: 197844 - isotretinoin 20 MG Oral Capsule
- RxCUI: 197845 - ISOtretinoin 40 MG Oral Capsule
- RxCUI: 197845 - isotretinoin 40 MG Oral Capsule
- RxCUI: 403930 - ISOtretinoin 30 MG Oral Capsule
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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".