NDC 61877-0006 Somaderm
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 61877-0006?
What are the uses for Somaderm?
Which are Somaderm UNII Codes?
The UNII codes for the active ingredients in this product are:
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (Active Moiety)
- THYROID, BOVINE (UNII: MN18OTN73W)
- THYROID, BOVINE (UNII: MN18OTN73W) (Active Moiety)
- SOMATROPIN (UNII: NQX9KB6PCL)
- SOMATROPIN (UNII: NQX9KB6PCL) (Active Moiety)
Which are Somaderm 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)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- SORBIC ACID (UNII: X045WJ989B)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- LICORICE (UNII: 61ZBX54883)
- CHASTE TREE (UNII: 433OSF3U8A)
- EPIMEDIUM SAGITTATUM TOP (UNII: 7G8Y7M4D58)
- GINKGO (UNII: 19FUJ2C58T)
- MUCUNA PRURIENS SEED (UNII: 55G8SQ543S)
- DIOSCOREA VILLOSA TUBER (UNII: IWY3IWX2G8)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
- PEG-8 DIMETHICONE (UNII: GIA7T764OD)
- POLYETHYLENE GLYCOL 700 (UNII: 762678AC5R)
- TOCOPHEROL (UNII: R0ZB2556P8)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- OREGANO (UNII: 0E5AT8T16U)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
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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".