NDC 61805-090 Orbel
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 61805-090?
What are the uses for Orbel?
Which are Orbel UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Orbel 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- MEGLUMINE (UNII: 6HG8UB2MUY)
- HYDROXYETHYL CELLULOSE (4000 MPA.S AT 1%) (UNII: ZYD53NBL45)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- .ALPHA.-AMYLCINNAMALDEHYDE (UNII: WC51CA3418)
- .ALPHA.-AMYLCINNAMYL ALCOHOL (UNII: DKB52S61GU)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- BENZYL BENZOATE (UNII: N863NB338G)
- CITRAL (UNII: T7EU0O9VPP)
- .BETA.-CITRONELLOL, (+/-)- (UNII: 565OK72VNF)
- COUMARIN (UNII: A4VZ22K1WT)
- EUGENOL (UNII: 3T8H1794QW)
- GERANIOL (UNII: L837108USY)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- HYDROXYISOHEXYL 3-CYCLOHEXENE CARBOXALDEHYDE (UNII: QUE43B9Z2Q)
- HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- EVERNIA PRUNASTRI (UNII: O3034Q5AHK)
- PSEUDEVERNIA FURFURACEA (UNII: 49ZMN09Q0K)
What is the NDC to RxNorm Crosswalk for Orbel?
- RxCUI: 1052530 - ethanol 72 % Topical Solution
- RxCUI: 1052530 - ethanol 0.72 ML/ML Topical Solution
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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".