NDC 50090-0768 Clindamycin Phosphate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 50090-0768?
What are the uses for Clindamycin Phosphate?
Which are Clindamycin Phosphate UNII Codes?
The UNII codes for the active ingredients in this product are:
- CLINDAMYCIN PHOSPHATE (UNII: EH6D7113I8)
- CLINDAMYCIN (UNII: 3U02EL437C) (Active Moiety)
Which are Clindamycin Phosphate 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:
- ALLANTOIN (UNII: 344S277G0Z)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
- CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: HHT01ZNK31)
What is the NDC to RxNorm Crosswalk for Clindamycin Phosphate?
- RxCUI: 2676585 - clindamycin phosphate 1 % Twice-Daily Topical Gel
- RxCUI: 2676585 - Twice-Daily clindamycin 0.01 MG/MG Topical Gel
- RxCUI: 2676585 - clindamycin (as clindamycin phosphate) 1 % Twice-Daily Topical Gel
* Please review the disclaimer below.
Patient Education
Clindamycin Topical
Topical clindamycin is used to treat acne. Clindamycin is in a class of medications called lincomycin antibiotics. It works by slowing or stopping the growth of bacteria that cause acne and by decreasing swelling.
[Learn More]
* 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".