NDC 54868-4806 Clindamycin Phosphate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-4806 - Clindamycin Phosphate
Product Packages
NDC Code 54868-4806-0
Package Description: 1 BOTTLE in 1 CARTON / 60 mL in 1 BOTTLE
Product Details
What is NDC 54868-4806?
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:
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- ISOSTEARYL ALCOHOL (UNII: Q613OCQ44Y)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- METHYLPARABEN (UNII: A2I8C7HI9T)
What is the NDC to RxNorm Crosswalk for Clindamycin Phosphate?
- RxCUI: 197519 - clindamycin phosphate 1 % Topical Lotion
- RxCUI: 197519 - clindamycin 10 MG/ML Topical Lotion
- RxCUI: 197519 - clindamycin (as clindamycin phosphate) 1 % Topical Lotion
- RxCUI: 197519 - clindamycin 1 % Topical Lotion
- RxCUI: 2676585 - clindamycin phosphate 1 % Twice-Daily Topical Gel
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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".