NDC 47046-151 Bacitracin Zinc
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 47046 - Anicare Pharmaceuticals Pvt. Ltd
- 47046-151 - Bacitracin Zinc
Product Packages
NDC Code 47046-151-02
Package Description: 1 TUBE in 1 CARTON / 14 g in 1 TUBE (47046-151-01)
Product Details
What is NDC 47046-151?
What are the uses for Bacitracin Zinc?
Which are Bacitracin Zinc UNII Codes?
The UNII codes for the active ingredients in this product are:
- BACITRACIN ZINC (UNII: 89Y4M234ES)
- BACITRACIN (UNII: 58H6RWO52I) (Active Moiety)
Which are Bacitracin Zinc 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)
- WHITE PETROLATUM (UNII: B6E5W8RQJ4)
What is the NDC to RxNorm Crosswalk for Bacitracin Zinc?
- 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.
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* 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".