NDC 51367-006 Fengliaoxing Fengshi Dieda Yaojiu
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51367 - International Nature Nutraceuticals
- 51367-006 - Fengliaoxing Fengshi Dieda Yaojiu
Product Packages
NDC Code 51367-006-25
Package Description: 1 LIQUID in 1 BOTTLE
Product Details
What is NDC 51367-006?
What are the uses for Fengliaoxing Fengshi Dieda Yaojiu?
Which are Fengliaoxing Fengshi Dieda Yaojiu UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Fengliaoxing Fengshi Dieda Yaojiu 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:
- ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)
- GLEDITSIA SINENSIS FRUIT (UNII: A6W0J6UO7Q)
- TANGERINE PEEL (UNII: JU3D414057)
- ATRACTYLODES LANCEA ROOT (UNII: CAZ6282J2O)
- CYPERUS ROTUNDUS ROOT (UNII: 4B51SRR959)
- CITRUS AURANTIUM FRUIT, IMMATURE (UNII: NOV6870B68)
- ATRACTYLODES MACROCEPHALA ROOT (UNII: 08T3N29QJB)
- CUSCUTA CHINENSIS SEED (UNII: 77SZY178UD)
- FENNEL (UNII: 557II4LLC3)
- PRUNUS ARMENIACA SEED (UNII: 75356789IW)
- ALISMA PLANTAGO-AQUATICA SUBSP. ORIENTALE ROOT (UNII: 555C7I140L)
- MYRRH (UNII: JC71GJ1F3L)
- LIGUSTICUM WALLICHII ROOT (UNII: R81AD159QS)
- ANGELICA SINENSIS ROOT (UNII: B66F4574UG)
- FRANKINCENSE (UNII: R9XLF1R1WM)
- PAEONIA SUFFRUTICOSA ROOT BARK (UNII: BUG255FE7X)
- CULLEN CORYLIFOLIUM FRUIT (UNII: 78AD6Z52S6)
- POLYGONATUM SIBIRICUM ROOT (UNII: O6N69G5Q18)
- CHINESE YAM (UNII: 29CIF30B1Z)
- CHINESE CINNAMON (UNII: WS4CQ062KM)
* 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".