NDC 52380-1274 Aplicare Antiseptic Chlorhexidine Gluconate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52380 - Aplicare, Inc.
- 52380-1274 - Aplicare Antiseptic Chlorhexidine Gluconate
Product Packages
NDC Code 52380-1274-4
Package Description: 120 g in 1 BOTTLE
NDC Code 52380-1274-6
Package Description: 480 g in 1 BOTTLE
NDC Code 52380-1274-7
Package Description: 960 g in 1 BOTTLE
NDC Code 52380-1274-8
Package Description: 240 g in 1 BOTTLE
NDC Code 52380-1274-9
Package Description: 3785 g in 1 BOTTLE
Product Details
What is NDC 52380-1274?
What are the uses for Aplicare Antiseptic Chlorhexidine Gluconate?
Which are Aplicare Antiseptic Chlorhexidine Gluconate UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)
- CHLORHEXIDINE (UNII: R4KO0DY52L) (Active Moiety)
Which are Aplicare Antiseptic Chlorhexidine Gluconate 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:
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- COCAMIDE DIETHANOLAMINE (UNII: 92005F972D)
- HYDROXYETHYL CELLULOSE (140 CPS AT 5%) (UNII: 8136Y38GY5)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Aplicare Antiseptic Chlorhexidine Gluconate?
- RxCUI: 834152 - chlorhexidine gluconate 2 % Topical Solution
- RxCUI: 834152 - chlorhexidine gluconate 20 MG/ML Topical Solution
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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".