NDC 73405-101 Body Derm
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 73405-101?
What are the uses for Body Derm?
Which are Body Derm UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
Which are Body Derm 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)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- XYLITYLGLUCOSIDE (UNII: O0IEZ166FB)
- ANHYDROXYLITOL (UNII: 8XWR7NN42F)
- XYLITOL (UNII: VCQ006KQ1E)
- POTASSIUM AZELOYL DIGLYCINATE (UNII: N02RVN6NYP)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- HEDYCHIUM CORONARIUM ROOT (UNII: 92A6N0IQN9)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- TRANSFORMING GROWTH FACTOR BETA RECEPTOR TYPE 3 (UNII: 18YWT2KYS8)
- URTICA DIOICA SUBSP. DIOICA LEAF (UNII: 232L6DS3Y4)
- SALIX ALBA WHOLE (UNII: V8UV0R324S)
- LINDEN LEAF (UNII: RU6O456OJ1)
- YUCCA SCHIDIGERA ROOT (UNII: E2H9ET15AT)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CUCUMBER (UNII: YY7C30VXJT)
- HYALURONIC ACID (UNII: S270N0TRQY)
- RESVERATROL (UNII: Q369O8926L)
- GINKGO (UNII: 19FUJ2C58T)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- SOMATROPIN (UNII: NQX9KB6PCL)
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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".