BoneArth Care

Manufacturer
Dong woo dang pharmacy Co.,Ltd.
Effective date
2021-09-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:42:23

Label at a glance#

ProductBoneArth Care
Active ingredientACHYRANTHES BIDENTATA WHOLE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Achyranthes bidentata Blume

OTC - PURPOSE SECTION

anti aging
Osteoblast production

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

Take 3 times a day

WARNINGS SECTION

■ For external use only.

■ Do not use in eyes.

■ lf swallowed, get medical help promptly.

■ Stop use, ask doctor lf irritation occurs.

■ Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

for external use only

INACTIVE INGREDIENT SECTION

Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82230-0001-12024-01-30C16284748780-11030e365-5aab-111a-e063-dadaa90a10e2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82230-0001-1BoneArth Care100 mL in 1 POUCHLIQUID1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82230-0001BONEARTH CARE (ACHYRANTHES BIDENTATA BLUME) LIQUID [DONG WOO DANG PHARMACY CO.,LTD.]1Legacy NDC, 1 package rows20210915_cbaeac9d-cdcf-3d0e-e053-2995a90a57b4.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82230-000182230-0001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ACHYRANTHES BIDENTATA WHOLE0B5LIZ2V2HACTIB
WATER059QF0KO0RIACT

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
cbaeac99-b3b5-8eb2-e053-2a95a90ac863cbaeac9d-cdcf-3d0e-e053-2995a90a57b42021-09-10WarningsExact identifier
spl id: cbaeac99-b3b5-8eb2-e053-2a95a90ac863
spl set id: cbaeac9d-cdcf-3d0e-e053-2995a90a57b4

Reported adverse events (FAERS/openFDA)#

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