NDC 90108-050 Handsanitizer Antibacterial Gel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 90108 - Bathletix
- 90108-050 - Handsanitizer
Product Packages
NDC Code 90108-050-00
Package Description: 1 LIQUID in 1 BOTTLE
Product Details
What is NDC 90108-050?
What are the uses for Handsanitizer Antibacterial Gel?
Which are Handsanitizer Antibacterial Gel UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Handsanitizer Antibacterial Gel 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)
- GUARAPROLOSE (1300 MPA.S AT 1%) (UNII: 1530WMS90S)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- MATRICARIA CHAMOMILLA WHOLE (UNII: G0R4UBI2ZZ)
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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".