NDC 72934-1018 Benzoyl Peroxide 5% / Clindamycin 1% / Niacinamide 2% / Tretinoin 0.1%
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72934 - Sincerus Florida, Llc
- 72934-1018 - Benzoyl Peroxide 5% / Clindamycin 1% / Niacinamide 2% / Tretinoin 0.1%
Product Characteristics
Product Packages
NDC Code 72934-1018-2
Package Description: 30 g in 1 BOTTLE, PUMP
Product Details
What is NDC 72934-1018?
Which are Benzoyl Peroxide 5% / Clindamycin 1% / Niacinamide 2% / Tretinoin 0.1% UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM)
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (Active Moiety)
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
- CLINDAMYCIN PHOSPHATE (UNII: EH6D7113I8)
- CLINDAMYCIN (UNII: 3U02EL437C) (Active Moiety)
- TRETINOIN (UNII: 5688UTC01R)
- TRETINOIN (UNII: 5688UTC01R) (Active Moiety)
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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".