SSANGGI TANG

Manufacturer
LYDIA Co., Ltd | I World Pharmaceutical Co., Ltd
Effective date
2019-10-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:01:16

Label at a glance#

ProductSSANGGI TANG
Active ingredientPAEONIA LACTIFLORA ROOT, REHMANNIA GLUTINOSA ROOT, LIGUSTICUM SINENSE SUBSP. CHUANXIONG ROOT, ASTRAGALUS GUMMIFER ROOT
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ssanghwa extract (peony root, rehmannia root, cnidium rhizome, astragalus root, angelica gias root, cinnamon bark, licorice, raw ginger, jujube)

OTC - PURPOSE SECTION

for cure fatigue, physical weakness, and illness such as cold sweats

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INDICATIONS & USAGE SECTION

take 1 pouch 3 times a day

WARNINGS SECTION

do not intake if the product is found to have expired or corrupted

when using this product be aware that the contents may flow when opening

stop use and ask a doctor if you have certain body types and allergies, it can cause a severe allergic reaction

INACTIVE INGREDIENT SECTION

water, liquid fructose

DOSAGE & ADMINISTRATION SECTION

For oral use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72988-0022-12021-01-29C16284748780-1ba0f9c33-4827-a910-e053-dadaa90a0b8595493d64-b312-6ba2-e053-2995a90ab04b

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72988-0022-1SSANGGI TANG80 mL in 1 POUCHLIQUID801

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72988-0022SSANGGI TANG (SSANGHWA EXTRACT) LIQUID [LYDIA CO., LTD]1Legacy NDC, 1 package rows20191020_95493d64-b312-6ba2-e053-2995a90ab04b.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72988-002272988-0022-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
95494fe5-4800-d36f-e053-2a95a90a13ff95493d64-b312-6ba2-e053-2995a90ab04b2019-10-19WarningsExact identifier
spl id: 95494fe5-4800-d36f-e053-2a95a90a13ff
spl set id: 95493d64-b312-6ba2-e053-2995a90ab04b

Reported adverse events (FAERS/openFDA)#

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