NDC 75983-004 First Aid Antibiotic Bacitraycin Plus Maximum Strength
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75983 - First Aid Research Corp.
- 75983-004 - First Aid Antibiotic Bacitraycin Plus Maximum Strength
Product Packages
NDC Code 75983-004-28
Package Description: 1 TUBE in 1 CARTON / 28 g in 1 TUBE
Product Details
What is NDC 75983-004?
What are the uses for First Aid Antibiotic Bacitraycin Plus Maximum Strength?
Which are First Aid Antibiotic Bacitraycin Plus Maximum Strength UNII Codes?
The UNII codes for the active ingredients in this product are:
- BACITRACIN (UNII: 58H6RWO52I)
- BACITRACIN (UNII: 58H6RWO52I) (Active Moiety)
- PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5)
- PRAMOXINE (UNII: 068X84E056) (Active Moiety)
Which are First Aid Antibiotic Bacitraycin Plus Maximum Strength 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)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- MINERAL OIL (UNII: T5L8T28FGP)
- PETROLATUM (UNII: 4T6H12BN9U)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
What is the NDC to RxNorm Crosswalk for First Aid Antibiotic Bacitraycin Plus Maximum Strength?
- RxCUI: 1303727 - bacitracin 500 UNT / pramoxine HCl 10 MG per GM Topical Ointment
- RxCUI: 1303727 - bacitracin 0.5 UNT/MG / pramoxine hydrochloride 0.01 MG/MG Topical Ointment
- RxCUI: 1303727 - bacitracin 500 UNT / pramoxine hydrochloride 10 MG 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".