NDC 82570-018 Detangjiang
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 82570 - Shenzhen Deyintang Biotechnology Co., Ltd.
- 82570-018 - Detangjiang
Product Packages
NDC Code 82570-018-01
Package Description: 3 g in 1 POUCH
Product Details
What is NDC 82570-018?
What are the uses for Detangjiang?
Which are Detangjiang UNII Codes?
The UNII codes for the active ingredients in this product are:
- COLLAGEN, SOLUBLE, FISH SKIN (UNII: 8JC99XGU4W)
- COLLAGEN, SOLUBLE, FISH SKIN (UNII: 8JC99XGU4W) (Active Moiety)
- SELENIUM (UNII: H6241UJ22B)
- SELENIUM (UNII: H6241UJ22B) (Active Moiety)
- CHROMIUM (UNII: 0R0008Q3JB)
- CHROMIUM (UNII: 0R0008Q3JB) (Active Moiety)
- MAGNESIUM OXIDE (UNII: 3A3U0GI71G)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- ZINC GLUCONATE (UNII: U6WSN5SQ1Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
- MORINGA OLEIFERA LEAF (UNII: 4WET1AWO9B)
- MORINGA OLEIFERA LEAF (UNII: 4WET1AWO9B) (Active Moiety)
- BIDENS PILOSA LEAF (UNII: 457932TMZ8)
- BIDENS PILOSA LEAF (UNII: 457932TMZ8) (Active Moiety)
- MOMORDICA CHARANTIA WHOLE (UNII: 83M15WOS0F)
- MOMORDICA CHARANTIA WHOLE (UNII: 83M15WOS0F) (Active Moiety)
Which are Detangjiang 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:
- BLUEBERRY (UNII: 253RUG1X1A)
- MALIC ACID (UNII: 817L1N4CKP)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CRANBERRY (UNII: 0MVO31Q3QS)
* 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".