NDC 69790-641 Hand Wash
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69790 - Uline
- 69790-641 - Hand Wash
Product Packages
NDC Code 69790-641-96
Package Description: 221 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 69790-641?
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)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)
- MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)
- PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- EDETATE SODIUM (UNII: MP1J8420LU)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C RED NO. 4 (UNII: X3W0AM1JLX)
What is the NDC to RxNorm Crosswalk for Hand Wash?
- RxCUI: 1233282 - benzalkonium chloride 0.1 % Medicated Liquid Soap
- RxCUI: 1233282 - benzalkonium chloride 1 MG/ML Medicated Liquid Soap
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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".