NDC 58737-217 My Little Pony Hand Sanitizer Set
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58737 - Townley Inc.
- 58737-217 - My Little Pony Hand Sanitizer Set
Product Characteristics
GRAPE (C73391)
BUBBLE GUM (C73368)
BLUEBERRY (C73367)
WATERMELON (C73423)
STRAWBERRY (C73417)
Product Packages
NDC Code 58737-217-01
Package Description: 59 g in 1 BOTTLE
Product Details
What is NDC 58737-217?
What are the uses for My Little Pony Hand Sanitizer Set?
Which are My Little Pony Hand Sanitizer Set UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are My Little Pony Hand Sanitizer Set 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:
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- COCETH-7 (UNII: 58Y261JLH5)
- PPG-1-PEG-9 LAURYL GLYCOL ETHER (UNII: 5R8J43K25L)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
What is the NDC to RxNorm Crosswalk for My Little Pony Hand Sanitizer Set?
- RxCUI: 1049228 - benzalkonium chloride 0.1 % Topical Gel
- RxCUI: 1049228 - benzalkonium chloride 0.001 MG/MG Topical Gel
* 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".