NDC 80308-002 B-protek
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 80308-002-01
Package Description: 3 mL in 1 POUCH
NDC Code 80308-002-02
Package Description: 30 mL in 1 BOTTLE, PLASTIC
NDC Code 80308-002-03
Package Description: 60 mL in 1 BOTTLE, PLASTIC
NDC Code 80308-002-04
Package Description: 250 mL in 1 BOTTLE, PLASTIC
NDC Code 80308-002-05
Package Description: 500 mL in 1 BOTTLE, PLASTIC
NDC Code 80308-002-06
Package Description: 1000 mL in 1 BOTTLE, PLASTIC
NDC Code 80308-002-07
Package Description: 3785 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 80308-002?
What are the uses for B-protek?
Which are B-protek 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 B-protek 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)
- CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- WATER (UNII: 059QF0KO0R)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- TROLAMINE (UNII: 9O3K93S3TK)
What is the NDC to RxNorm Crosswalk for B-protek?
- RxCUI: 2397699 - isopropyl alcohol 80 % Topical Gel
- RxCUI: 2397699 - isopropyl alcohol 0.8 ML/ML Topical Gel
* Please review the disclaimer below.
[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".