NDC 50069-201 Suave Essentials - Antibacterial Deeply Clean Refreshing Deodorant Bar
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50069 - Unilever Asia Private Limited
- 50069-201 - Suave Essentials - Antibacterial Deeply Clean Refreshing Deodorant Bar
Product Packages
NDC Code 50069-201-12
Package Description: 2 NOT APPLICABLE in 1 CARTON / 112 g in 1 NOT APPLICABLE
Product Details
What is NDC 50069-201?
What are the uses for Suave Essentials - Antibacterial Deeply Clean Refreshing Deodorant Bar?
Which are Suave Essentials - Antibacterial Deeply Clean Refreshing Deodorant Bar UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Suave Essentials - Antibacterial Deeply Clean Refreshing Deodorant Bar 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:
- SODIUM PALMATE (UNII: S0A6004K3Z)
- SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- EDETATE SODIUM (UNII: MP1J8420LU)
- ETIDRONIC ACID (UNII: M2F465ROXU)
- ALCOHOL (UNII: 3K9958V90M)
- BENZYL SALICYLATE (UNII: WAO5MNK9TU)
- COUMARIN (UNII: A4VZ22K1WT)
- LINALOOL, (+)- (UNII: F4VNO44C09)
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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".