NDC 54868-4497 Retin-a Micro
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-4497 - Retin-a Micro
Product Packages
NDC Code 54868-4497-0
Package Description: 1 TUBE in 1 CARTON / 20 g in 1 TUBE
NDC Code 54868-4497-1
Package Description: 1 TUBE in 1 CARTON / 45 g in 1 TUBE
Product Details
What is NDC 54868-4497?
What are the uses for Retin-a Micro?
Which are Retin-a Micro UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRETINOIN (UNII: 5688UTC01R)
- TRETINOIN (UNII: 5688UTC01R) (Active Moiety)
Which are Retin-a Micro 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:
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- CARBOMER HOMOPOLYMER TYPE B (UNII: HHT01ZNK31)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- SORBIC ACID (UNII: X045WJ989B)
- TROLAMINE (UNII: 9O3K93S3TK)
What is the NDC to RxNorm Crosswalk for Retin-a Micro?
- RxCUI: 313453 - tretinoin 0.1 % Topical Gel
- RxCUI: 313453 - tretinoin 0.001 MG/MG Topical Gel
- RxCUI: 359050 - tretinoin 0.04 % Topical Gel
- RxCUI: 359050 - tretinoin 0.0004 MG/MG Topical Gel
- RxCUI: 805370 - RETIN-A MICRO 0.04 % Topical Gel
* 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".