NDC 65923-390 Uec Medical First Aid Antibiotic
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 65923 - United Exchange Corp.
- 65923-390 - Uec Medical First Aid Antibiotic
Product Packages
NDC Code 65923-390-20
Package Description: 20 PACKET in 1 BOX / .9 g in 1 PACKET
NDC Code 65923-390-44
Package Description: 144 PACKET in 1 BOX / .9 g in 1 PACKET
Product Details
What is NDC 65923-390?
What are the uses for Uec Medical First Aid Antibiotic?
Which are Uec Medical First Aid Antibiotic UNII Codes?
The UNII codes for the active ingredients in this product are:
- BACITRACIN ZINC (UNII: 89Y4M234ES)
- BACITRACIN (UNII: 58H6RWO52I) (Active Moiety)
Which are Uec Medical First Aid Antibiotic 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:
- PARAFFIN (UNII: I9O0E3H2ZE)
- MINERAL OIL (UNII: T5L8T28FGP)
What is the NDC to RxNorm Crosswalk for Uec Medical First Aid Antibiotic?
- RxCUI: 1366116 - bacitracin zinc 500 UNT/GM Topical Ointment
- RxCUI: 1366116 - bacitracin zinc 0.5 UNT/MG Topical Ointment
- RxCUI: 1366116 - bacitracin zinc 500 UNT per GM Topical Ointment
* Please review the disclaimer below.
Patient Education
Bacitracin Topical
Bacitracin is used to help prevent minor skin injuries such as cuts, scrapes, and burns from becoming infected. Bacitracin is in a class of medications called antibiotics. Bacitracin works by stopping the growth of bacteria.
[Learn More]
* 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".