FDA.reportPublic FDA data

T-dol JIANG SUAN BAO

Manufacturer
Shenzhen Hanyuanhe Cultural Health Industry Development Co., Ltd.
Effective date
2019-11-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:11:32

Label at a glance#

ProductT-dol JIANG SUAN BAO
Active ingredientFOLIC ACID
Label structure8 sections

Label contents#

Full prescribing information#

WARNINGS SECTION

This product contains soy and its products, used with caution for allergies

INACTIVE INGREDIENT SECTION

Noni, Xiaoben Hongling Grass, Green South African Dr. Tea, Patented Fermented Daphnia Extract, Chrysanthemum Polyphenols, Guava, Sour Cherry

INDICATIONS & USAGE SECTION

Add 150ml of water at room temperature every time, shake it and use it.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHIL DREN SECTION

OTC - PURPOSE SECTION

Supplement the protein needed by the human body

OTC - ACTIVE INGREDIENT SECTION

Folic acid

DOSAGE & ADMINISTRATION SECTION

Every time a bag, every day...

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
91c62db0-0295-c81c-d10a-0856c259edd6Product name220200428
d32bc2b8-0bb7-2216-87aa-24639646e202Product name320190619

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75018-004-012021-01-29C16284748780-1ba0f9c33-292c-a910-e053-dadaa90a0b85966d1783-cad7-92cb-e053-2995a90a7db4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75018-004-01T-dol JIANG SUAN BAO5 g in 1 POUCHPOWDER51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75018-004T-DOL JIANG SUAN BAO (SOLID POWDER) POWDER [SHENZHEN HANYUANHE CULTURAL HEALTH INDUSTRY DEVELOPMENT CO., LTD.]1Legacy NDC, 1 package rows20191103_966d1783-cad7-92cb-e053-2995a90a7db4.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75018-00475018-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
SOUR CHERRY1L29G6428XIACT
NOLINIUMRA7HHG7F9HIACT
ASPALATHUS LINEARIS WHOLEO17JQA1A9ZIACT
GUAVA74O70D6VG0IACT
FOLIC ACID935E97BOY8ACTIB
PLATOSTOMA PALUSTRE WHOLEFE70D062O9IACT
BARLEY5PWM7YLI7RIACT
CHRYSANTHEMIN8X15R84UEMIACT

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
966d1783-cad8-92cb-e053-2995a90a7db4966d1783-cad7-92cb-e053-2995a90a7db42019-11-03WarningsExact identifier
spl id: 966d1783-cad8-92cb-e053-2995a90a7db4
spl set id: 966d1783-cad7-92cb-e053-2995a90a7db4

Reported adverse events (FAERS/openFDA)#

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