NDC 44224-3300 After Cuts And Scrapes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 44224-3300?
What are the uses for After Cuts And Scrapes?
Which are After Cuts And Scrapes UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
- IBUPROFEN (UNII: WK2XYI10QM)
- IBUPROFEN (UNII: WK2XYI10QM) (Active Moiety)
- ASPIRIN (UNII: R16CO5Y76E)
- ASPIRIN (UNII: R16CO5Y76E) (Active Moiety)
- DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40)
- DIPHENHYDRAMINE (UNII: 8GTS82S83M) (Active Moiety)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
- AMMONIA (UNII: 5138Q19F1X)
- AMMONIA (UNII: 5138Q19F1X) (Active Moiety)
Which are After Cuts And Scrapes 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:
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- GLYCERIN (UNII: PDC6A3C0OX)
- MENTHOL (UNII: L7T10EIP3A)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
- TALC (UNII: 7SEV7J4R1U)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- STARCH, CORN (UNII: O8232NY3SJ)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- MINERAL OIL (UNII: T5L8T28FGP)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- D&C RED NO. 27 (UNII: 2LRS185U6K)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SORBITOL (UNII: 506T60A25R)
- WATER (UNII: 059QF0KO0R)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- POVIDONE (UNII: FZ989GH94E)
- LIGHT MINERAL OIL (UNII: N6K5787QVP)
- DIMETHICONE 1000 (UNII: MCU2324216)
- C12-13 ALCOHOLS (UNII: T7ZJT3I9X2)
What is the NDC to RxNorm Crosswalk for After Cuts And Scrapes?
- RxCUI: 1009433 - lidocaine HCl 2.5 % Topical Gel
- RxCUI: 1009433 - lidocaine hydrochloride 0.025 MG/MG Topical Gel
- RxCUI: 1009433 - lidocaine hydrochloride 2.5 % Topical Gel
- RxCUI: 1049630 - diphenhydrAMINE HCl 25 MG Oral Tablet
- RxCUI: 1049630 - diphenhydramine hydrochloride 25 MG Oral Tablet
* Please review the disclaimer below.
[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".