NDC 55319-431 Modesa Moisturizing Hand Antibacterial
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55319 - Family Dollar Services Inc.
- 55319-431 - Modesa
Product Packages
NDC Code 55319-431-40
Package Description: 1180 mL in 1 BOTTLE, PLASTIC
NDC Code 55319-431-75
Package Description: 221 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 55319-431?
What are the uses for Modesa Moisturizing Hand Antibacterial?
Which are Modesa Moisturizing Hand Antibacterial UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZETHONIUM CHLORIDE (UNII: PH41D05744)
- BENZETHONIUM (UNII: 1VU15B70BP) (Active Moiety)
Which are Modesa Moisturizing Hand Antibacterial 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)
- LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
- COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- EDETATE SODIUM (UNII: MP1J8420LU)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Modesa Moisturizing Hand Antibacterial?
- RxCUI: 1053207 - benzethonium chloride 0.1 % Medicated Liquid Soap
- RxCUI: 1053207 - benzethonium chloride 1 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".