NDC 54868-5991 Epiduo
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5991 - Epiduo
Product Packages
NDC Code 54868-5991-0
Package Description: 1 TUBE in 1 CARTON / 45 g in 1 TUBE
Product Details
What is NDC 54868-5991?
What are the uses for Epiduo?
Which are Epiduo UNII Codes?
The UNII codes for the active ingredients in this product are:
- ADAPALENE (UNII: 1L4806J2QF)
- ADAPALENE (UNII: 1L4806J2QF) (Active Moiety)
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM)
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (Active Moiety)
Which are Epiduo 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:
- DOCUSATE SODIUM (UNII: F05Q2T2JA0)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- POLOXAMER 124 (UNII: 1S66E28KXA)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
What is the NDC to RxNorm Crosswalk for Epiduo?
- RxCUI: 829539 - adapalene 0.1 % / benzoyl peroxide 2.5 % Topical Gel
- RxCUI: 829539 - adapalene 0.001 MG/MG / benzoyl peroxide 0.025 MG/MG Topical Gel
- RxCUI: 830648 - Epiduo 0.1 % / 2.5 % Topical Gel
- RxCUI: 830648 - adapalene 0.001 MG/MG / benzoyl peroxide 0.025 MG/MG Topical Gel [Epiduo]
- RxCUI: 830648 - Epiduo (adapalene 0.1 % / benzoyl peroxide 2.5 %) 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".