NDC 79097-020 Affex Care Ultra Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 79097 - Autotrol Corporation
- 79097-020 - Affex Care Ultra Hand Sanitizer
Product Packages
NDC Code 79097-020-01
Package Description: 50 mL in 1 BOTTLE, PLASTIC
NDC Code 79097-020-02
Package Description: 59 mL in 1 BOTTLE, PLASTIC
NDC Code 79097-020-03
Package Description: 100 mL in 1 BOTTLE, PLASTIC
NDC Code 79097-020-04
Package Description: 118 mL in 1 BOTTLE, PLASTIC
NDC Code 79097-020-08
Package Description: 237 mL in 1 BOTTLE, PLASTIC
NDC Code 79097-020-12
Package Description: 355 mL in 1 BOTTLE, PLASTIC
NDC Code 79097-020-16
Package Description: 473 mL in 1 BOTTLE, PLASTIC
NDC Code 79097-020-28
Package Description: 3785 mL in 1 BOTTLE, PLASTIC
NDC Code 79097-020-75
Package Description: 1000000 mL in 1 TANK
Product Details
What is NDC 79097-020?
What are the uses for Affex Care Ultra Hand Sanitizer?
What is the NDC to RxNorm Crosswalk for Affex Care Ultra Hand Sanitizer?
- RxCUI: 581662 - ethanol 70 % Topical Gel
- RxCUI: 581662 - ethanol 0.7 ML/ML Topical Gel
- RxCUI: 581662 - ethyl alcohol 70 % Topical Gel
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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".