NDC 43333-454 Antibacterial Foaming Hand Wash Sweet Treats
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43333 - Tonic Bath And Body Products Shenzhen Ltd.
- 43333-454 - Antibacterial Foaming Hand Wash Sweet Treats
Product Packages
NDC Code 43333-454-16
Package Description: 500 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 43333-454?
What are the uses for Antibacterial Foaming Hand Wash Sweet Treats?
Which are Antibacterial Foaming Hand Wash Sweet Treats UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Antibacterial Foaming Hand Wash Sweet Treats 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- CITRIC ACID ACETATE (UNII: DSO12WL7AU)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)
- WATER (UNII: 059QF0KO0R)
- EDETIC ACID (UNII: 9G34HU7RV0)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- GLYCERIN (UNII: PDC6A3C0OX)
- WITCH HAZEL (UNII: 101I4J0U34)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- OLEA EUROPAEA LEAF (UNII: MJ95C3OH47)
- PANTHENOL (UNII: WV9CM0O67Z)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM LAURAMINOPROPIONATE (UNII: X5NJA9HXPU)
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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".