FDA.reportPublic FDA data

HANTAI 8030 Ca-D3 Premium

Manufacturer
APEXEL CO., LTD.
Effective date
2015-06-01
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 22:42:37

Label at a glance#

ProductHANTAI 8030 Ca-D3 Premium
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 disorders, depression, nerve 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

WARNINGS

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.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

For oral use only

USES

INDICATIONS & USAGE SECTION

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

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hantai 8030 Ca-D3 PremiumHantai 8030 Ca-D3 Premium

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
55259-4001-22020-01-31C16284748780-19d75b9d0-c89e-f424-e053-dadaa90a57ce15d3e602-d44b-057d-e054-00144ff8d46c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55259-4001-2HANTAI 8030 Ca-D3 Premium120 in 1 BOTTLETABLET1203
55259-4001-2HANTAI 8030 Ca-D3 Premium1 in 1 PACKAGETABLET13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55259-4001HANTAI 8030 CA-D3 PREMIUM (OSTREAE CONCHA, CALCIUM) TABLET [APEXEL CO., LTD.]3Legacy NDC, 2 package rows20150602_15d3e602-d44b-057d-e054-00144ff8d46c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CALCIUMACTIVE INGREDIENTSY7Q814VUP3
CALCIUMACTIVE MOIETYSY7Q814VUP3
GERMANIUMINACTIVE INGREDIENT00072J7XWS3
IRONINACTIVE INGREDIENTE1UOL152H73
MAGNESIUMINACTIVE INGREDIENTI38ZP9992A3
MANGANESEINACTIVE INGREDIENT42Z2K6ZL8P3
POTASSIUMINACTIVE INGREDIENTRWP5GA015D3
SELENIUMINACTIVE INGREDIENTH6241UJ22B3
ZINC OXIDEINACTIVE INGREDIENTSOI2LOH54Z3

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
55259-400155259-4001-2

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
ZINC OXIDESOI2LOH54ZIACT
CALCIUMSY7Q814VUPACTIB
MAGNESIUMI38ZP9992AIACT
SELENIUMH6241UJ22BIACT
GERMANIUM00072J7XWSIACT
IRONE1UOL152H7IACT
POTASSIUMRWP5GA015DIACT
MANGANESE42Z2K6ZL8PIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 7 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ZINC OXIDEZINC OXIDESOI2LOH54ZSUPPOSITORY / RECTAL375 mgExact identifier — unii candidate
6 equally ranked IID candidates
IRONIRONE1UOL152H7TABLET, EXTENDED RELEASE / ORAL5 mgExact identifier — unii candidate
ZINC OXIDEZINC OXIDESOI2LOH54ZSOLUTION / RESPIRATORY (INHALATION)3.11 %w/vExact identifier — unii candidate
6 equally ranked IID candidates
ZINC OXIDEZINC OXIDESOI2LOH54ZINJECTION, SUSPENSION / SUBCUTANEOUSNAExact identifier — unii candidate
6 equally ranked IID candidates
ZINC OXIDEZINC OXIDESOI2LOH54ZLOTION / TOPICAL16 %w/wExact identifier — unii candidate
6 equally ranked IID candidates
ZINC OXIDEZINC OXIDESOI2LOH54ZSOLUTION / INTRAVENOUS3.11 %w/vExact identifier — unii candidate
6 equally ranked IID candidates
ZINC OXIDEZINC OXIDESOI2LOH54ZINJECTION / SUBCUTANEOUS0.02 %w/vExact identifier — unii candidate
6 equally ranked IID candidates

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
177b5794-db5b-48e5-e054-00144ff88e8815d3e602-d44b-057d-e054-00144ff8d46c2015-06-01WarningsExact identifier
spl id: 177b5794-db5b-48e5-e054-00144ff88e88
spl set id: 15d3e602-d44b-057d-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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