BAENOSIN

Manufacturer
Lydia Co., Ltd. | I World Pharmaceutical Co., Ltd.
Effective date
2023-12-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:04:44

Label at a glance#

ProductBAENOSIN
Active ingredientLICORICE, PAEONIA LACTIFLORA ROOT, PLATYCODON GRANDIFLORUM ROOT, JUJUBE FRUIT, GINGER, PONCIRUS TRIFOLIATA FRUIT
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

platycodon root, licorice, jujube, peony root, ginger, poncirus immature fruit

INACTIVE INGREDIENT SECTION

lactose monohydrate, acacia, corn starch, carboxymethylcellulose calcium, l-menthol

OTC - PURPOSE SECTION

pyrogenic diseases with redness, swelling, stiffness and pain

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

adults take 2 capsules 3 times a day before meals or between meals

WARNINGS SECTION

do not take this medicine if you have following symptoms

symptoms of headaches, chills, and fever other than local symptoms such as spasm (red with blood), swelling, and pain at the same time

DOSAGE & ADMINISTRATION SECTION

for oral use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
GINGER Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72988-0011-12023-12-16C16284748780-1ba0f9c33-4f8e-a910-e053-dadaa90a0b85Drug Facts
72988-0011-12021-01-29C16284748780-1ba0f9c33-4f8e-a910-e053-dadaa90a0b85Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72988-0011-1BAENOSIN10 in 1 PACKAGECAPSULE102

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72988-0011BAENOSIN (PLATYCODON ROOT, LICORICE, JUJUBE, PEONY ROOT) CAPSULE [LYDIA CO., LTD.]2Current NDC, Legacy NDC, 1 package rows20231217_874f9b81-80eb-05fd-e053-2a95a90afdeb.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72988-001172988-0011-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
BAENOSINPLATYCODON ROOT, LICORICE, JUJUBE, PEONY ROOTLydia Co., Ltd.874f9b81-80eb-05fd-e053-2a95a90afdeb2023-12-16WarningsExact identifier
ndc (package): 72988-0011-1
ndc (product): 72988-0011
ndc11 (package): 72988001101
spl id: 0ca8ac22-aaab-9d25-e063-6294a90a4541
spl set id: 874f9b81-80eb-05fd-e053-2a95a90afdeb

Reported adverse events (FAERS/openFDA)#

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