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HANTAI 8030 Ca-D3 Premium

Medically reviewed on Jun 1, 2018

Dosage form: tablet
Ingredients: CALCIUM 0.991
Labeler: APEXEL CO., LTD.
NDC Code: 55259-4001

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

ACTIVE INGREDIENT

Ostreae Concha (Calcium 99%)

INACTIVE INGREDIENT

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

PURPOSE

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

Keep out of Reach of Children

WARNINGS

  • 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

For oral use only

USES

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

PACKAGE LABEL

HANTAI 8030 CA-D3 PREMIUM 
ostreae concha, calcium tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55259-4001
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CALCIUM (CALCIUM) CALCIUM0.99 
Inactive Ingredients
Ingredient NameStrength
ZINC OXIDE 
MAGNESIUM 
SELENIUM 
GERMANIUM 
IRON 
POTASSIUM 
MANGANESE 
Product Characteristics
ColorwhiteScorescore with uneven pieces
ShapeOVALSize12mm
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:55259-4001-21 BOTTLE in 1 PACKAGE
1120 TABLET in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other05/18/2015
Labeler - APEXEL CO., LTD. (687287979)
Registrant - APEXEL CO., LTD. (687287979)
Establishment
NameAddressID/FEIOperations
APEXEL CO., LTD.687287979manufacture(55259-4001)

 
APEXEL CO., LTD.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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