NDC 76113-012 American Infection Control Antiseptic Hand Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76113 - American Infection Control, Inc.
- 76113-012 - American Infection Control Antiseptic Hand Wipes
Product Packages
NDC Code 76113-012-25
Package Description: 12 CANISTER in 1 CASE / 385 mL in 1 CANISTER
NDC Code 76113-012-54
Package Description: 20 PACKAGE in 1 CASE / 228 mL in 1 PACKAGE
Product Details
What is NDC 76113-012?
What are the uses for American Infection Control Antiseptic Hand Wipes?
Which are American Infection Control Antiseptic Hand Wipes UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are American Infection Control Antiseptic Hand 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)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for American Infection Control Antiseptic Hand Wipes?
- RxCUI: 1041780 - ethanol 62 % Medicated Pad
- RxCUI: 1041780 - ethanol 0.62 ML/ML Medicated Pad
- RxCUI: 1041780 - ethanol 62 % Hand Sanitizer Wipes
- RxCUI: 1041780 - ethanol 62 % Topical Cloth
- RxCUI: 1041780 - ethanol 62 % Topical Swab
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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".