NDC 80479-175 Bernal Premium Alcohol Wipe
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 80479 - Newport Mfg Llc
- 80479-175 - Bernal Premium Alcohol Wipe
Product Packages
NDC Code 80479-175-01
Package Description: 3 mL in 1 POUCH
NDC Code 80479-175-15
Package Description: 15 POUCH in 1 BOX / 3 mL in 1 POUCH
NDC Code 80479-175-40
Package Description: 40 POUCH in 1 BOX / 3 mL in 1 POUCH
NDC Code 80479-175-99
Package Description: 100 POUCH in 1 BAG / 3 mL in 1 POUCH
Product Details
What is NDC 80479-175?
What are the uses for Bernal Premium Alcohol Wipe?
Which are Bernal Premium Alcohol Wipe UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Bernal Premium Alcohol Wipe 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:
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GLYCERIN (UNII: PDC6A3C0OX)
- LEMON OIL (UNII: I9GRO824LL)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Bernal Premium Alcohol Wipe?
- RxCUI: 1307051 - ethanol 75 % Medicated Pad
- RxCUI: 1307051 - ethanol 0.75 ML/ML Medicated Pad
- RxCUI: 1307051 - ethanol 75 % Hand Sanitizer Wipes
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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".