NDC 51852-100 First Aid Triple Antibiotic And Pain Relief Maximum Strength
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51852 - Lifelabs, A Division Of Atico International Usa, Inc.
- 51852-100 - First Aid Triple Antibiotic And Pain Relief
Product Characteristics
Product Packages
NDC Code 51852-100-01
Package Description: 1 TUBE in 1 CARTON / 28 g in 1 TUBE
Product Details
What is NDC 51852-100?
What are the uses for First Aid Triple Antibiotic And Pain Relief Maximum Strength?
Which are First Aid Triple Antibiotic And Pain Relief Maximum Strength UNII Codes?
The UNII codes for the active ingredients in this product are:
- BACITRACIN ZINC (UNII: 89Y4M234ES)
- BACITRACIN (UNII: 58H6RWO52I) (Active Moiety)
- NEOMYCIN SULFATE (UNII: 057Y626693)
- NEOMYCIN (UNII: I16QD7X297) (Active Moiety)
- POLYMYXIN B SULFATE (UNII: 19371312D4)
- POLYMYXIN B (UNII: J2VZ07J96K) (Active Moiety)
- PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5)
- PRAMOXINE (UNII: 068X84E056) (Active Moiety)
Which are First Aid Triple Antibiotic And Pain Relief 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:
- MINERAL OIL (UNII: T5L8T28FGP)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- PETROLATUM (UNII: 4T6H12BN9U)
What is the NDC to RxNorm Crosswalk for First Aid Triple Antibiotic And Pain Relief Maximum Strength?
- RxCUI: 1359350 - bacitracin 500 UNT / neomycin 3.5 MG / polymyxin B 10,000 UNT / pramoxine HCl 10 MG per GM Topical Ointment
- RxCUI: 1359350 - bacitracin 0.5 UNT/MG / neomycin 0.0035 MG/MG / polymyxin B 10 UNT/MG / pramoxine hydrochloride 0.01 MG/MG 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".