NDC 72197-029 Pharmacys Prescription Alcohol Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72197 - American Consumer Products Corp
- 72197-029 - Pharmacys Prescription Alcohol Wipes
Product Packages
NDC Code 72197-029-10
Package Description: 10 mL in 1 BAG
NDC Code 72197-029-50
Package Description: 50 mL in 1 BAG
NDC Code 72197-029-80
Package Description: 80 mL in 1 BAG
Product Details
What is NDC 72197-029?
What are the uses for Pharmacys Prescription Alcohol Wipes?
Which are Pharmacys Prescription 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 Pharmacys Prescription 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYL GLYCERIN ACETAL LEVULINATE (UNII: 7233JH4G65)
- COCO DIETHANOLAMIDE (UNII: 92005F972D)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- WATER (UNII: 059QF0KO0R)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
What is the NDC to RxNorm Crosswalk for Pharmacys Prescription 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".