NDC 72265-104 Quash Multi Sanitizing Tissue
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72265 - Curescript
- 72265-104 - Quash Multi Sanitizing Tissue
Product Packages
NDC Code 72265-104-01
Package Description: 20 CLOTH in 1 PACKET
Product Details
What is NDC 72265-104?
What are the uses for Quash Multi Sanitizing Tissue?
Which are Quash Multi Sanitizing Tissue UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Quash Multi Sanitizing Tissue 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)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- MENTHOL (UNII: L7T10EIP3A)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- POLOXAMER 184 (UNII: BIS92ZSF57)
- PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- THYME (UNII: CW657OBU4N)
- SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
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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".