NDC 69842-383 Hand Wash
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69842 - Cvs Pharmacy
- 69842-383 - Hand Wash
Product Packages
NDC Code 69842-383-81
Package Description: 332 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 69842-383?
What are the uses for Hand Wash?
Which are Hand Wash UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Hand Wash 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)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)
- GLYCERIN (UNII: PDC6A3C0OX)
- DISTEARETH-75 ISOPHORONE DIISOCYANATE (UNII: 5365FJ30SC)
- PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- EDETATE SODIUM (UNII: MP1J8420LU)
- SULISOBENZONE (UNII: 1W6L629B4K)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
What is the NDC to RxNorm Crosswalk for Hand Wash?
- 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".