NDC 74758-007 And Bobs Your Uncle Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 74758 - Ambrose Cubed Llc
- 74758-007 - And Bobs Your Uncle Hand Sanitizer
Product Packages
NDC Code 74758-007-01
Package Description: 59 mL in 1 BOTTLE
NDC Code 74758-007-02
Package Description: 118 mL in 1 BOTTLE
NDC Code 74758-007-03
Package Description: 236 mL in 1 BOTTLE
NDC Code 74758-007-04
Package Description: 473 mL in 1 BOTTLE
NDC Code 74758-007-05
Package Description: 1000 mL in 1 BOTTLE
NDC Code 74758-007-08
Package Description: 3785 mL in 1 BOTTLE
Product Details
What is NDC 74758-007?
What are the uses for And Bobs Your Uncle Hand Sanitizer?
Which are And Bobs Your Uncle Hand Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL ALCOHOL (UNII: ND2M416302) (Active Moiety)
Which are And Bobs Your Uncle 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 And Bobs Your Uncle Hand Sanitizer?
- RxCUI: 1039900 - isopropyl alcohol 75 % Topical Solution
- RxCUI: 1039900 - isopropyl alcohol 0.75 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".