NDC 81877-300 Triadime
Triamcinolone Acetonide Cream .1%,Dimethicone 5% Cream Kit - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 81877-300?
What are the uses for Triadime?
Which are Triadime UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRIAMCINOLONE ACETONIDE (UNII: F446C597KA)
- TRIAMCINOLONE ACETONIDE (UNII: F446C597KA) (Active Moiety)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Triadime 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)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SORBITOL (UNII: 506T60A25R)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- SORBIC ACID (UNII: X045WJ989B)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- WATER (UNII: 059QF0KO0R)
- GELIDIELLA ACEROSA (UNII: T91K54D6M1)
- METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y)
- HONEY (UNII: Y9H1V576FH)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
- SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H)
- OMEGA-3 FATTY ACIDS (UNII: 71M78END5S)
- PHYTONADIONE (UNII: A034SE7857)
- ORANGE OIL (UNII: AKN3KSD11B)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD)
- RAPESEED STEROL (UNII: B46B6DD20U)
- HYDROLYZED SOY PROTEIN (ENZYMATIC; 2000 MW) (UNII: 1394NXB9L6)
- CORN OIL (UNII: 8470G57WFM)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- CARTHAMUS TINCTORIUS SEED OLEOSOMES (UNII: 9S60Q72309)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- PEG-100 STEARATE (UNII: YD01N1999R)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- COCONUT OIL (UNII: Q9L0O73W7L)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
- CLOVE (UNII: K48IKT5321)
- MANDARIN OIL (UNII: NJO720F72R)
- GRAPEFRUIT OIL (UNII: YR377U58W9)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PROPANEDIOL (UNII: 5965N8W85T)
- CETYLHYDROXYPROLINE PALMITAMIDE (UNII: 74ONU0S62G)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- HEXYLDECANOL (UNII: 151Z7P1317)
- .BETA.-BISABOLOL (UNII: LP618AV2EA)
- 7-DEHYDROCHOLESTEROL (UNII: BK1IU07GKF)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- VANILLIN (UNII: CHI530446X)
What is the NDC to RxNorm Crosswalk for Triadime?
- RxCUI: 1014314 - triamcinolone acetonide 0.1 % Topical Cream
- RxCUI: 1014314 - triamcinolone acetonide 1 MG/ML Topical Cream
- RxCUI: 1014314 - triamcinolone acetonide 1 MG per GM Topical Cream
- RxCUI: 259090 - dimethicone 5 % Topical Cream
- RxCUI: 259090 - dimethicone 50 MG/ML Topical Cream
* 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".