NDC 74897-001 Doctor Daves Autosan Hs Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 74897 - Automated Chemical Solutions, Inc.
- 74897-001 - Doctor Daves Autosan Hs Hand Sanitizer
Product Packages
NDC Code 74897-001-01
Package Description: 3785 mL in 1 BOTTLE
NDC Code 74897-001-05
Package Description: 18925 mL in 1 BAG
NDC Code 74897-001-08
Package Description: 237 mL in 1 BOTTLE
NDC Code 74897-001-16
Package Description: 473 mL in 1 BOTTLE
NDC Code 74897-001-32
Package Description: 946 mL in 1 BOTTLE
NDC Code 74897-001-55
Package Description: 207000 mL in 1 DRUM
Product Details
What is NDC 74897-001?
What are the uses for Doctor Daves Autosan Hs Hand Sanitizer?
Which are Doctor Daves Autosan Hs 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 Doctor Daves Autosan Hs 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Doctor Daves Autosan Hs Hand Sanitizer?
- RxCUI: 1039339 - ethanol 80 % Topical Solution
- RxCUI: 1039339 - ethanol 0.8 ML/ML Topical Solution
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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".