NDC 75749-051 Alcohol Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 75749-051-01
Package Description: 1 CONTAINER in 1 CONTAINER / 5 mL in 1 CONTAINER
NDC Code 75749-051-02
Package Description: 2 CONTAINER in 1 CONTAINER / 10 mL in 1 CONTAINER
NDC Code 75749-051-03
Package Description: 10 CONTAINER in 1 CONTAINER / 1 CONTAINER in 1 CONTAINER / 5 mL in 1 CONTAINER
NDC Code 75749-051-04
Package Description: 12 CONTAINER in 1 CONTAINER / 1 CONTAINER in 1 CONTAINER / 5 mL in 1 CONTAINER
NDC Code 75749-051-05
Package Description: 20 CONTAINER in 1 CONTAINER / 1 CONTAINER in 1 CONTAINER / 5 mL in 1 CONTAINER
NDC Code 75749-051-06
Package Description: 24 CONTAINER in 1 CONTAINER / 1 CONTAINER in 1 CONTAINER / 5 mL in 1 CONTAINER
NDC Code 75749-051-07
Package Description: 30 CONTAINER in 1 CONTAINER / 1 CONTAINER in 1 CONTAINER / 5 mL in 1 CONTAINER
NDC Code 75749-051-08
Package Description: 40 CONTAINER in 1 CONTAINER / 1 CONTAINER in 1 CONTAINER / 5 mL in 1 CONTAINER
NDC Code 75749-051-09
Package Description: 48 CONTAINER in 1 CONTAINER / 1 CONTAINER in 1 CONTAINER / 5 mL in 1 CONTAINER
NDC Code 75749-051-10
Package Description: 50 CONTAINER in 1 CONTAINER / 1 CONTAINER in 1 CONTAINER / 5 mL in 1 CONTAINER
NDC Code 75749-051-11
Package Description: 100 CONTAINER in 1 CONTAINER / 1 CONTAINER in 1 CONTAINER / 5 mL in 1 CONTAINER
NDC Code 75749-051-12
Package Description: 10 CONTAINER in 1 CONTAINER / 2 CONTAINER in 1 CONTAINER / 10 mL in 1 CONTAINER
NDC Code 75749-051-13
Package Description: 12 CONTAINER in 1 CONTAINER / 2 CONTAINER in 1 CONTAINER / 10 mL in 1 CONTAINER
NDC Code 75749-051-14
Package Description: 20 CONTAINER in 1 CONTAINER / 2 CONTAINER in 1 CONTAINER / 10 mL in 1 CONTAINER
NDC Code 75749-051-15
Package Description: 24 CONTAINER in 1 CONTAINER / 2 CONTAINER in 1 CONTAINER / 10 mL in 1 CONTAINER
NDC Code 75749-051-16
Package Description: 30 CONTAINER in 1 CONTAINER / 2 CONTAINER in 1 CONTAINER / 10 mL in 1 CONTAINER
NDC Code 75749-051-17
Package Description: 40 CONTAINER in 1 CONTAINER / 2 CONTAINER in 1 CONTAINER / 10 mL in 1 CONTAINER
NDC Code 75749-051-18
Package Description: 48 CONTAINER in 1 CONTAINER / 2 CONTAINER in 1 CONTAINER / 10 mL in 1 CONTAINER
NDC Code 75749-051-19
Package Description: 50 CONTAINER in 1 CONTAINER / 2 CONTAINER in 1 CONTAINER / 10 mL in 1 CONTAINER
NDC Code 75749-051-20
Package Description: 100 CONTAINER in 1 CONTAINER / 2 CONTAINER in 1 CONTAINER / 10 mL in 1 CONTAINER
Product Details
What is NDC 75749-051?
What are the uses for Alcohol Wipes?
Which are Alcohol Wipes UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Alcohol Wipes 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)
- WATER (UNII: 059QF0KO0R)
- ALOE (UNII: V5VD430YW9)
What is the NDC to RxNorm Crosswalk for Alcohol Wipes?
- RxCUI: 1307051 - ethanol 75 % Medicated Pad
- RxCUI: 1307051 - ethanol 0.75 ML/ML Medicated Pad
- RxCUI: 1307051 - ethanol 75 % Hand Sanitizer Wipes
* 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".