NDC 72042-003 Burn Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72042 - Humn Pharmaceuticals Inc
- 72042-003 - Burn Relief
Product Characteristics
Product Packages
NDC Code 72042-003-03
Package Description: 1 TUBE in 1 CARTON / 28300 mg in 1 TUBE
Product Details
What is NDC 72042-003?
What are the uses for Burn Relief?
Which are Burn Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- LIDOCAINE HYDROCHLORIDE ANHYDROUS (UNII: EC2CNF7XFP)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
Which are Burn Relief 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:
- CETETH-20 (UNII: I835H2IHHX)
- ALCOHOL (UNII: 3K9958V90M)
- ALUMINUM DICETYL PHOSPHATE (UNII: WMV3R5DS7O)
- GLYCERIN (UNII: PDC6A3C0OX)
- MINERAL OIL (UNII: T5L8T28FGP)
- PEG-6 STEARATE (UNII: 8LQC57C6B0)
- PEG-100 STEARATE (UNII: YD01N1999R)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- STEARETH-2 (UNII: V56DFE46J5)
- STEARETH-20 (UNII: L0Q8IK9E08)
- CETETH-10 PHOSPHATE (UNII: 4E05O5N49G)
- PEG-120 GLYCERYL STEARATE (UNII: 6941286E4I)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- LAURETH-7 (UNII: Z95S6G8201)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- DIMETHICONE 100 (UNII: RO266O364U)
- POLYSORBATE 85 (UNII: A7F3N56197)
- WATER (UNII: 059QF0KO0R)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- ACRYLAMIDE (UNII: 20R035KLCI)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- .ALPHA.-LIPOIC ACID (UNII: 73Y7P0K73Y)
- STEARETH-21 (UNII: 53J3F32P58)
What is the NDC to RxNorm Crosswalk for Burn Relief?
- RxCUI: 2045344 - allantoin 1.5 % / lidocaine HCl 4 % / menthol 1 % Topical Cream
- RxCUI: 2045344 - allantoin 15 MG/ML / lidocaine hydrochloride 40 MG/ML / menthol 10 MG/ML Topical Cream
* 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".