NDC 61767-220 Bacitracin Zinc
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61767 - Blossom Pharmaceuticals
- 61767-220 - Bacitracin Zinc
Product Packages
NDC Code 61767-220-01
Package Description: .9 g in 1 PACKET
NDC Code 61767-220-02
Package Description: 28.35 g in 1 TUBE
NDC Code 61767-220-03
Package Description: 14.17 g in 1 TUBE
NDC Code 61767-220-04
Package Description: 113.4 g in 1 TUBE
NDC Code 61767-220-05
Package Description: .5 g in 1 PACKET
NDC Code 61767-220-07
Package Description: 425.3 g in 1 JAR
Product Details
What is NDC 61767-220?
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:
- PETROLATUM (UNII: 4T6H12BN9U)
- LIGHT MINERAL OIL (UNII: N6K5787QVP)
- MINERAL OIL (UNII: T5L8T28FGP)
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
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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".