NDC 72686-184 Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72686 - Fareva Morton Grove, Inc.
- 72686-184 - Hand Sanitizer
Product Packages
NDC Code 72686-184-05
Package Description: 50 mL in 1 TUBE
Product Details
What is NDC 72686-184?
What are the uses for Hand Sanitizer?
Which are 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 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:
- CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- AGAR, UNSPECIFIED (UNII: 89T13OHQ2B)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- GLYCERIN (UNII: PDC6A3C0OX)
- FRAGRANCE FLORAL ORC0902236 (UNII: R66Z4YW3X0)
- WATER (UNII: 059QF0KO0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- GELLAN GUM (LOW ACYL) (UNII: 7593U09I4D)
- CALCIUM ALGINATE (UNII: 8P20S56HZI)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ULTRAMARINE BLUE (UNII: I39WR998BI)
What is the NDC to RxNorm Crosswalk for Hand Sanitizer?
- RxCUI: 1788839 - ethanol 77 % Topical Gel
- RxCUI: 1788839 - ethanol 0.77 ML/ML 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".