83582-001 NDC - RHINITIS YITULING (PORIA,GLYCYRRHIZA URALENSIS,MANDARIN PEEL, ATRACTYLODES MACROCEPHALA,DIOSCOREA OPPOSITA,JUJUBE,HONEY,MENTHAE,XANTHIUM,MAGNOLIA CITRIODORA FLOWER BUD)

Drug Information

Product NDC: 83582-001

Proprietary Name: Rhinitis Yituling

Non Proprietary Name: PORIA,GLYCYRRHIZA URALENSIS,MANDARIN PEEL, ATRACTYLODES MACROCEPHALA,DIOSCOREA OPPOSITA,JUJUBE,HONEY,MENTHAE,XANTHIUM,MAGNOLIA CITRIODORA FLOWER BUD

Active Ingredient(s):
  • 7 g/100g ATRACTYLODES MACROCEPHALA WHOLE;
  • 12 g/100g CHINESE YAM;
  • 18 g/100g FU LING;
  • 9 g/100g GLYCYRRHIZA URALENSIS;
  • 3 g/100g HONEY;
  • 2 g/100g JUJUBE FRUIT;
  • 3 g/100g MAGNOLIA DENUDATA FLOWER BUD;
  • 6 g/100g MENTHA ARVENSIS LEAF;
  • 7 g/100g TANGERINE PEEL;
  • 5 g/100g XANTHIUM SIBIRICUM FRUIT


Administration Route(s): NASAL

Dosage Form(s): GEL

Labeler Information

Labeler Name: Sanfutang Traditional Chinese Medicine Investment (Yunnan) Co., Ltd
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:7/27/2023

Package Information

No. Package Code Package Description Billing Unit
183582-001-012 BOTTLE in 1 BOX (83582-001-01) / 5 g in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC83582-001The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMERhinitis YitulingThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEPORIA,GLYCYRRHIZA URALENSIS,MANDARIN PEEL, ATRACTYLODES MACROCEPHALA,DIOSCOREA OPPOSITA,JUJUBE,HONEY,MENTHAE,XANTHIUM,MAGNOLIA CITRIODORA FLOWER BUDThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEGELThe translation of the dosage form Code submitted by the firm.
ROUTE NAMENASALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE7/27/2023This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED DRUG OTHERProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMESanfutang Traditional Chinese Medicine Investment (Yunnan) Co., LtdName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEATRACTYLODES MACROCEPHALA WHOLE; CHINESE YAM; FU LING; GLYCYRRHIZA URALENSIS; HONEY; JUJUBE FRUIT; MAGNOLIA DENUDATA FLOWER BUD; MENTHA ARVENSIS LEAF; TANGERINE PEEL; XANTHIUM SIBIRICUM FRUITAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH7; 12; 18; 9; 3; 2; 3; 6; 7; 5 
ACTIVE INGRED UNITg/100g; g/100g; g/100g; g/100g; g/100g; g/100g; g/100g; g/100g; g/100g; g/100g 

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This page was last updated on: 10/12/2023