NDC 43853-0008 Adrenal And Dhea
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43853 - Problen
- 43853-0008 - Adrenal And Dhea
Product Packages
NDC Code 43853-0008-3
Package Description: 1 CARTON in 1 CARTON / 1 BOTTLE, SPRAY in 1 CARTON (43853-0008-2) / 30 mL in 1 BOTTLE, SPRAY (43853-0008-1)
Product Details
What is NDC 43853-0008?
What are the uses for Adrenal And Dhea?
Which are Adrenal And Dhea UNII Codes?
The UNII codes for the active ingredients in this product are:
- AMERICAN GINSENG (UNII: 8W75VCV53Q)
- AMERICAN GINSENG (UNII: 8W75VCV53Q) (Active Moiety)
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (Active Moiety)
- SILYBUM MARIANUM SEED (UNII: U946SH95EE)
- SILYBUM MARIANUM SEED (UNII: U946SH95EE) (Active Moiety)
- PRASTERONE (UNII: 459AG36T1B)
- PRASTERONE (UNII: 459AG36T1B) (Active Moiety)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (Active Moiety)
- ARGININE (UNII: 94ZLA3W45F)
- ARGININE (UNII: 94ZLA3W45F) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
- THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786)
- THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786) (Active Moiety)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) (Active Moiety)
Which are Adrenal And Dhea 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)
- ALCOHOL (UNII: 3K9958V90M)
* Please review the disclaimer below.
[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".