Rhinitis Yituling

Manufacturer
Sanfutang Traditional Chinese Medicine Investment (Yunnan) Co., Ltd
Effective date
2023-07-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:55:45

Label at a glance#

ProductRhinitis Yituling
Active ingredientTANGERINE PEEL, XANTHIUM SIBIRICUM FRUIT, ATRACTYLODES MACROCEPHALA WHOLE, CHINESE YAM, JUJUBE FRUIT, HONEY, MENTHA ARVENSIS LEAF, FU LING, GLYCYRRHIZA URALENSIS, MAGNOLIA DENUDATA FLOWER BUD
Label structure9 sections

Indications and uses

This product is used to relieve various discomfort caused by nasal itching, nasal congestion, runny nose, sneezing, and nasal swelling

Dosage and administration

1.Under 2 years of age should be used under the guidance of a doctor 2.2 to adults once a day, severe symptoms twice, no more than 3 times 3.Apply this product directly or spray it to the nasal cavity

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

PORIA, GLYCYRRHIZA URALENSIS, MANDARIN PEEL, ATRACTYLODES MACROCEPHALA, DIOSCOREA OPPOSITA, JUJUBE

, HONEY, MENTHAE, XANTHIUM, MAGNOLIA CITRIODORA FLOWER BUD

peurpose

OTC - PURPOSE SECTION

clearing away the lung-heat、Dredging the nasal cavity、Reduce swelling and relieve pain

Uses

INDICATIONS & USAGE SECTION

This product is used to relieve various discomfort caused by nasal itching, nasal congestion, runny nose, sneezing, and nasal swelling

Warnings

WARNINGS SECTION

1.This product is for external use, and internal service is prohibited

2.Children need to be used under adult supervision

3.Stop using this product when allergic or causing itching

4.The product is discontinued when the odor and character change

If pregnant or breastfeeding

LACTATION SECTION

Consult with a health professional before use

Stay away from children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If you overdose, seek medical help or contact a poison control center

Directions

DOSAGE & ADMINISTRATION SECTION

1.Under 2 years of age should be used under the guidance of a doctor

2.2 to adults once a day, severe symptoms twice, no more than 3 times

3.Apply this product directly or spray it to the nasal cavity

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerol, water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SFTSFT

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83582-001-012025-01-30C16284748780-12cef2736-60db-d83d-e063-dadaa90ab31f017262ec-1b29-b6d5-e063-6394a90aded7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83582-001-01Rhinitis Yituling2 in 1 BOXGEL21
83582-001-01Rhinitis Yituling5 g in 1 BOTTLEGEL51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83582-001RHINITIS YITULING (PORIA,GLYCYRRHIZA URALENSIS,MANDARIN PEEL, ATRACTYLODES MACROCEPHALA,DIOSCOREA OPPOSITA,JUJUBE,HONEY,MENTHAE,XANTHIUM,MAGNOLIA CITRIODORA FLOWER BUD) GEL [SANFUTANG TRADITIONAL CHINESE MEDICINE INVESTMENT (YUNNAN) CO., LTD]12 package rows20230729_017262ec-1b29-b6d5-e063-6394a90aded7.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83582-00183582-001-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
017262ec-1b2a-b6d5-e063-6394a90aded7017262ec-1b29-b6d5-e063-6394a90aded72023-07-27WarningsExact identifier
spl id: 017262ec-1b2a-b6d5-e063-6394a90aded7
spl set id: 017262ec-1b29-b6d5-e063-6394a90aded7

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.