NDC 82570-010 Dekangling
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 82570-010?
What are the uses for Dekangling?
Which are Dekangling UNII Codes?
The UNII codes for the active ingredients in this product are:
- CULTIVATED MUSHROOM (UNII: 54C8E6W6JY)
- CULTIVATED MUSHROOM (UNII: 54C8E6W6JY) (Active Moiety)
- CORDYCEPS MILITARIS FRUITING BODY (UNII: T1A06T9W4C)
- CORDYCEPS MILITARIS FRUITING BODY (UNII: T1A06T9W4C) (Active Moiety)
- MORINGA OLEIFERA LEAF (UNII: 4WET1AWO9B)
- MORINGA OLEIFERA LEAF (UNII: 4WET1AWO9B) (Active Moiety)
- COLLAGEN, SOLUBLE, FISH SKIN (UNII: 8JC99XGU4W)
- COLLAGEN, SOLUBLE, FISH SKIN (UNII: 8JC99XGU4W) (Active Moiety)
- POMIFERIN (UNII: 74YIS40APM)
- POMIFERIN (UNII: 74YIS40APM) (Active Moiety)
- TAIWANOFUNGUS CAMPHORATUS MYCELIUM (UNII: 233B609WYS)
- TAIWANOFUNGUS CAMPHORATUS MYCELIUM (UNII: 233B609WYS) (Active Moiety)
Which are Dekangling 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:
- LEMON (UNII: 24RS0A988O)
- MALIC ACID (UNII: 817L1N4CKP)
- CRANBERRY (UNII: 0MVO31Q3QS)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
* 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".