NDC 58264-0002 D2
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58264 - Dna Labs, Inc.
- 58264-0002 - D2
Product Packages
NDC Code 58264-0002-1
Package Description: 29.57 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 58264-0002?
What are the uses for D2?
Which are D2 UNII Codes?
The UNII codes for the active ingredients in this product are:
- GOLD TRICHLORIDE (UNII: 15443PR153)
- GOLD CATION (3+) (UNII: 7XM25QYI14) (Active Moiety)
- CRATAEGUS LAEVIGATA WHOLE (UNII: EFX9G567MJ)
- CRATAEGUS LAEVIGATA WHOLE (UNII: EFX9G567MJ) (Active Moiety)
- SELENICEREUS GRANDIFLORUS WHOLE (UNII: X8H7HS7MRM)
- SELENICEREUS GRANDIFLORUS WHOLE (UNII: X8H7HS7MRM) (Active Moiety)
- DIBASIC POTASSIUM PHOSPHATE (UNII: CI71S98N1Z)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- ACONITUM NAPELLUS (UNII: U0NQ8555JD)
- ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)
- VALERIANA OFFICINALIS WHOLE (UNII: FP6O7F1X9R)
- VALERIANA OFFICINALIS WHOLE (UNII: FP6O7F1X9R) (Active Moiety)
- SPIGELIA ANTHELMIA (UNII: WYT05213GE)
- SPIGELIA ANTHELMIA (UNII: WYT05213GE) (Active Moiety)
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- DIGITALIS PURPUREA WHOLE (UNII: UD4O8TY7RW)
- DIGITALIS PURPUREA WHOLE (UNII: UD4O8TY7RW) (Active Moiety)
- PRUNUS LAUROCERASUS WHOLE (UNII: 516S28LU0T)
- PRUNUS LAUROCERASUS WHOLE (UNII: 516S28LU0T) (Active Moiety)
- STRYCHNOS IGNATII WHOLE (UNII: 6YSJ329777)
- STRYCHNOS IGNATII WHOLE (UNII: 6YSJ329777) (Active Moiety)
Which are D2 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
* 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".