FDA.reportPublic FDA data

HANTAI 8030 Ca-D3 GOLD

Manufacturer
APEXEL CO., LTD.
Effective date
2021-03-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:39:04

Label at a glance#

ProductHANTAI 8030 Ca-D3 GOLD
Active ingredientCALCIUM
Label structure8 sections

Indications and uses

Take one tablet every time, two times a day with enough water.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Ostreae Concha (Calcium 99%)

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Magnesium, Zinc Oxide, Selenium, Germanium, Iron, Potassium, Manganese

PURPOSE

OTC - PURPOSE SECTION

To prevent and cure the osteoporosis, cardiovascular discorders, depression, verve stability, muscle pain, arthritis, menstrual pain, ostalgia and promote growth and healing.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

WARNING

WARNINGS SECTION

  • Please note it may choke during the intake tablets.
  • Please check product ingredients if you have any allergies before taking.
  • Please be careful during open the product package.
  • Keep product out of direct sunlight, high temperature and humidity.
  • Store in a cool dry place.
  • Keep out of reach of children.
  • Any items past the expiration date or damaged in transit can be exchanged where you originally purchased the item.

USES

DOSAGE & ADMINISTRATION SECTION

Take one tablet every time, two times a day with enough water.

INDICATION & USAGE SECTION

INDICATIONS & USAGE SECTION

For oral use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hantai 8030 Ca-D3 GoldHantai 8030 Ca-D3 Gold

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CALCIUM Pharmacologic Class Indexing3Indexing - Pharmacologic Class20230427

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
86fffa7b-d382-4771-a253-25cccb64b590Product name320251124
910c1bd7-67d1-44c7-ad4f-9445f827edccProduct name120230808
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55259-0004-12023-01-30C16284748780-1f386c64a-44c4-0266-e053-dadaa90a7c1abdc7a644-e86a-bf1d-e053-2995a90a1e03

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55259-0004-1HANTAI 8030 Ca-D3 GOLD120 in 1 BOTTLETABLET1201
55259-0004-1HANTAI 8030 Ca-D3 GOLD1 in 1 PACKAGETABLET11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55259-0004HANTAI 8030 CA-D3 GOLD (OSTREAE CONCHA (CALCIUM 99%)) TABLET [APEXEL CO., LTD.]1Legacy NDC, 2 package rows20210319_bdc7a644-e86a-bf1d-e053-2995a90a1e03.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
55259-000455259-0004-1

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
MAGNESIUMI38ZP9992AIACT
MANGANESE42Z2K6ZL8PIACT
GERMANIUM00072J7XWSIACT
IRONE1UOL152H7IACT
POTASSIUMRWP5GA015DIACT
ZINC OXIDESOI2LOH54ZIACT
SELENIUMH6241UJ22BIACT
CALCIUMSY7Q814VUPACTIB

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
bdc7a644-e869-bf1d-e053-2995a90a1e03bdc7a644-e86a-bf1d-e053-2995a90a1e032021-03-17WarningsExact identifier
spl id: bdc7a644-e869-bf1d-e053-2995a90a1e03
spl set id: bdc7a644-e86a-bf1d-e053-2995a90a1e03

Reported adverse events (FAERS/openFDA)#

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