NDC 72835-802 Duloxicaine
Duloxetine And Lidocaine Kit - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
WHITE (C48325 - WHITE BODY)
Code Structure Chart
Product Details
What is NDC 72835-802?
What are the uses for Duloxicaine?
Which are Duloxicaine UNII Codes?
The UNII codes for the active ingredients in this product are:
- DULOXETINE HYDROCHLORIDE (UNII: 9044SC542W)
- DULOXETINE (UNII: O5TNM5N07U) (Active Moiety)
- LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Duloxicaine 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:
- AMMONIA (UNII: 5138Q19F1X)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- GELATIN (UNII: 2G86QN327L)
- HYPROMELLOSE PHTHALATE (31% PHTHALATE, 40 CST) (UNII: G4U024CQK6)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SHELLAC (UNII: 46N107B71O)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- STARCH, CORN (UNII: O8232NY3SJ)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- ALLANTOIN (UNII: 344S277G0Z)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- ASTAXANTHIN (UNII: 8XPW32PR7I)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- BERGAMOT OIL (UNII: 39W1PKE3JI)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- CARBOMER INTERPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 132584PQMO)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE 200 (UNII: RGS4T2AS00)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- EDETATE SODIUM (UNII: MP1J8420LU)
- EMU OIL (UNII: 344821WD61)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- LAURETH-7 (UNII: Z95S6G8201)
- LEVOMENOL (UNII: 24WE03BX2T)
- N-ACETYL-GLUCOSAMINE THIAZOLINE (UNII: ML5FHL557A)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- POLYQUATERNIUM-10 (400 MPA.S AT 2%) (UNII: HB1401PQFS)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TEA TREE OIL (UNII: VIF565UC2G)
- TOCOPHEROL (UNII: R0ZB2556P8)
- TROLAMINE (UNII: 9O3K93S3TK)
- TURMERIC OIL (UNII: 6KGS8SP16U)
- VACCINIUM MYRTILLUS ANTHOCYANOSIDES (UNII: R911H793SU)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Duloxicaine?
- RxCUI: 1010895 - lidocaine HCl 4 % Topical Cream
- RxCUI: 1010895 - lidocaine hydrochloride 40 MG/ML Topical Cream
- RxCUI: 1010895 - lidocaine hydrochloride 4 % Topical Cream
- RxCUI: 2597529 - Lidocream Plus 4 % Topical Cream
- RxCUI: 2597529 - lidocaine hydrochloride 40 MG/ML Topical Cream [Lidocream]
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".