NDC 75710-078 Qb Skin Lab Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75710 - Quorum Bio Pharmaceutical Co., Ltd.
- 75710-078 - Qb Skin Lab Hand Sanitizer
Product Packages
NDC Code 75710-078-01
Package Description: 70 mL in 1 TUBE
Product Details
What is NDC 75710-078?
Which are Qb Skin Lab Hand Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Qb Skin Lab Hand Sanitizer 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:
- GALACTOSE (UNII: X2RN3Q8DNE)
- SODIUM ALGINATE (UNII: C269C4G2ZQ)
- POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIBASIC POTASSIUM PHOSPHATE (UNII: CI71S98N1Z)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- WATER (UNII: 059QF0KO0R)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ARGININE (UNII: 94ZLA3W45F)
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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".