NDC 75983-495 First Aid Macimum Sterngth Bacitraycin Plus
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75983 - First Aid Research Corp
- 75983-495 - First Aid Macimum Sterngth Bacitraycin Plus
Product Packages
NDC Code 75983-495-55
Package Description: 1 TUBE in 1 CARTON / 28 g in 1 TUBE
Product Details
What is NDC 75983-495?
What are the uses for First Aid Macimum Sterngth Bacitraycin Plus?
Which are First Aid Macimum Sterngth Bacitraycin Plus UNII Codes?
The UNII codes for the active ingredients in this product are:
- BACITRACIN (UNII: 58H6RWO52I)
- BACITRACIN (UNII: 58H6RWO52I) (Active Moiety)
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are First Aid Macimum Sterngth Bacitraycin Plus 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)
- MINERAL OIL (UNII: T5L8T28FGP)
- PETROLATUM (UNII: 4T6H12BN9U)
What is the NDC to RxNorm Crosswalk for First Aid Macimum Sterngth Bacitraycin Plus?
- RxCUI: 1490996 - bacitracin 500 UNT per GM / lidocaine HCl 40 MG per GM Topical Ointment
- RxCUI: 1490996 - bacitracin 0.5 UNT/MG / lidocaine hydrochloride 0.04 MG/MG Topical Ointment
- RxCUI: 1490996 - bacitracin 500 UNT per GM / lidocaine hydrochloride 40 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".