NDC 78851-333 Hand Gel Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 78851 - Allied Pressroom Products
- 78851-333 - Hand Gel Sanitizer
Product Packages
NDC Code 78851-333-01
Package Description: 105 mL in 1 BOTTLE, PLASTIC
NDC Code 78851-333-02
Package Description: 120 mL in 1 BOTTLE, PLASTIC
NDC Code 78851-333-03
Package Description: 240 mL in 1 BOTTLE, PLASTIC
NDC Code 78851-333-04
Package Description: 946 mL in 1 BOTTLE, PLASTIC
NDC Code 78851-333-05
Package Description: 3785 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 78851-333?
What are the uses for Hand Gel Sanitizer?
Which are Hand Gel 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 Gel 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:
- POLYETHYLENE GLYCOL 1000 (UNII: U076Q6Q621)
- ALLYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (LOW ALLYL METHACRYLATE) (UNII: PI80E777XB)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Hand Gel Sanitizer?
- RxCUI: 581662 - ethanol 70 % Topical Gel
- RxCUI: 581662 - ethanol 0.7 ML/ML Topical Gel
- RxCUI: 581662 - ethyl alcohol 70 % 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".