NDC 53943-114 Discount Drug Mart Antibacterial Foaming Fresh Water
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53943 - Discount Drug Mart
- 53943-114 - Discount Drug Mart
Product Packages
NDC Code 53943-114-07
Package Description: 222 mL in 1 BOTTLE, PLASTIC
NDC Code 53943-114-08
Package Description: 222 mL in 1 BOTTLE, PLASTIC
NDC Code 53943-114-31
Package Description: 946 mL in 1 BOTTLE, PLASTIC
NDC Code 53943-114-32
Package Description: 946 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 53943-114?
What are the uses for Discount Drug Mart Antibacterial Foaming Fresh Water?
Which are Discount Drug Mart Antibacterial Foaming Fresh Water UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Discount Drug Mart Antibacterial Foaming Fresh Water 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)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- GLYCERIN (UNII: PDC6A3C0OX)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
- XANTHAN GUM (UNII: TTV12P4NEE)
- EDETATE SODIUM (UNII: MP1J8420LU)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)
What is the NDC to RxNorm Crosswalk for Discount Drug Mart Antibacterial Foaming Fresh Water?
- RxCUI: 1046593 - benzalkonium chloride 0.13 % Medicated Liquid Soap
- RxCUI: 1046593 - benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap
- RxCUI: 1046593 - benzalkonium chloride 1.33 MG/ML Medicated Liquid 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".