NDC 53329-043 Skintegrity Antibacterial Hand Blue
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53329 - Medline Industries, Inc.
- 53329-043 - Skintegrity Antibacterial Hand
Product Packages
NDC Code 53329-043-20
Package Description: 1 BAG in 1 BOX / 800 mL in 1 BAG
Product Details
What is NDC 53329-043?
What are the uses for Skintegrity Antibacterial Hand Blue?
Which are Skintegrity Antibacterial Hand Blue UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Skintegrity Antibacterial Hand Blue 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:
- WATER (UNII: 059QF0KO0R)
- AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- COCO DIETHANOLAMIDE (UNII: 92005F972D)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- EDETATE SODIUM (UNII: MP1J8420LU)
- GLUTAMIC ACID (UNII: 3KX376GY7L)
- LEUCINE (UNII: GMW67QNF9C)
- SERINE (UNII: 452VLY9402)
- PHENYLALANINE (UNII: 47E5O17Y3R)
- PROLINE (UNII: 9DLQ4CIU6V)
- GLYCINE (UNII: TE7660XO1C)
- VALINE (UNII: HG18B9YRS7)
- ISOLEUCINE (UNII: 04Y7590D77)
- ARGININE (UNII: 94ZLA3W45F)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Skintegrity Antibacterial Hand Blue?
- RxCUI: 413247 - triclosan 0.5 % Medicated Liquid Soap
- RxCUI: 413247 - triclosan 5 MG/ML Medicated Liquid Soap
- RxCUI: 413247 - triclosan 0.5 % Foaming Medicated Hand Soap
* 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".