NDC 82570-011 Degong Ling
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 82570 - Shenzhen Deyintang Biotechnology Co., Ltd.
- 82570-011 - Degong Ling
Product Packages
NDC Code 82570-011-01
Package Description: 3 g in 1 POUCH
Product Details
What is NDC 82570-011?
What are the uses for Degong Ling?
Which are Degong Ling UNII Codes?
The UNII codes for the active ingredients in this product are:
- HIBISCUS SABDARIFFA CALYX (UNII: 584J2XT260)
- HIBISCUS SABDARIFFA CALYX (UNII: 584J2XT260) (Active Moiety)
- COLLAGEN, SOLUBLE, FISH SKIN (UNII: 8JC99XGU4W)
- COLLAGEN, SOLUBLE, FISH SKIN (UNII: 8JC99XGU4W) (Active Moiety)
Which are Degong Ling 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:
- BIFIDOBACTERIUM ANIMALIS LACTIS (UNII: 5307V7XW8I)
- LACTOBACILLUS PARACASEI (UNII: N1G291SC6Q)
- LACTOBACILLUS ACIDOPHILUS (UNII: 1PRR1V42V5)
- MALIC ACID (UNII: 817L1N4CKP)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- STREPTOCOCCUS THERMOPHILUS (UNII: T8F3MOB0CG)
- LACTOBACILLUS RHAMNOSUS (UNII: 9601IVB87J)
- BIFIDOBACTERIUM BIFIDUM (UNII: WN5C16297P)
- BIFIDOBACTERIUM LONGUM (UNII: 831AQW699W)
- CRANBERRY (UNII: 0MVO31Q3QS)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- LIMOSILACTOBACILLUS REUTERI (UNII: 9913I24QEE)
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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".