NDC 54860-121 Trolls Blueberry Scented Hand Sanitizer 01
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54860 - Shenzhen Lantern Science Co.,ltd.
- 54860-121 - Trolls Blueberry Scented Hand Sanitizer
Product Characteristics
BLUE (C48333)
BLUEBERRY (C73367)
Product Packages
NDC Code 54860-121-01
Package Description: 59 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54860-121?
What are the uses for Trolls Blueberry Scented Hand Sanitizer 01?
Which are Trolls Blueberry Scented Hand Sanitizer 01 UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Trolls Blueberry Scented Hand Sanitizer 01 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:
- COCETH-7 (UNII: 58Y261JLH5)
- PPG-1-PEG-9 LAURYL GLYCOL ETHER (UNII: 5R8J43K25L)
- WATER O-18 (UNII: 7QV8F8BYNJ)
- GLYCERIN (UNII: PDC6A3C0OX)
- CARBOMER 934 (UNII: Z135WT9208)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- MYRISTICA FRAGRANS FRUIT (UNII: GOO22BTU71)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
What is the NDC to RxNorm Crosswalk for Trolls Blueberry Scented Hand Sanitizer 01?
- RxCUI: 1049228 - benzalkonium chloride 0.1 % Topical Gel
- RxCUI: 1049228 - benzalkonium chloride 0.001 MG/MG Topical Gel
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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".