NDC 52124-1200 Genuine First Aid - Home First Aid
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
12 MM
AZ;235
Code Structure Chart
Product Details
What is NDC 52124-1200?
What are the uses for Genuine First Aid - Home First Aid?
Which are Genuine First Aid - Home First Aid 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)
- IBUPROFEN (UNII: WK2XYI10QM)
- IBUPROFEN (UNII: WK2XYI10QM) (Active Moiety)
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL ALCOHOL (UNII: ND2M416302) (Active Moiety)
Which are Genuine First Aid - Home First Aid 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:
- WATER (UNII: 059QF0KO0R)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- STARCH, CORN (UNII: O8232NY3SJ)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- LACTOSE (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYDEXTROSE (UNII: VH2XOU12IE)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- POVIDONE (UNII: FZ989GH94E)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
- CROSPOVIDONE (UNII: 68401960MK)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- MINERAL OIL (UNII: T5L8T28FGP)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- TALC (UNII: 7SEV7J4R1U)
What is the NDC to RxNorm Crosswalk for Genuine First Aid - Home First Aid?
- RxCUI: 1038561 - benzalkonium Cl 0.4 % Medicated Pad
- RxCUI: 1038561 - benzalkonium chloride 4 MG/ML Medicated Pad
- RxCUI: 1038561 - benzalkonium chloride 0.4 % Medicated Towelette
- RxCUI: 1038561 - benzalkonium chloride 0.4 % Topical Swab
- RxCUI: 198440 - acetaminophen 500 MG Oral Tablet
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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".