HANTAI 8030 CA-D3 GOLD (ostreae concha- calcium 99% tablet

HANTAI 8030 Ca-D3 GOLD by

Drug Labeling and Warnings

HANTAI 8030 Ca-D3 GOLD by is a Otc medication manufactured, distributed, or labeled by APEXEL CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ostreae Concha (Calcium 99%)

INACTIVE INGREDIENT

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

PURPOSE

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

Keep out of reach of children.

WARNING

• 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

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

INDICATION & USAGE SECTION

For oral use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HANTAI 8030 CA-D3 GOLD 
ostreae concha (calcium 99%) tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55259-5001
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CALCIUM (UNII: SY7Q814VUP) (CALCIUM - UNII:SY7Q814VUP)	CALCIUM	0.99

Inactive Ingredients
Ingredient Name	Strength
MAGNESIUM (UNII: I38ZP9992A)
MANGANESE (UNII: 42Z2K6ZL8P)
GERMANIUM (UNII: 00072J7XWS)
IRON (UNII: E1UOL152H7)
POTASSIUM (UNII: RWP5GA015D)
ZINC OXIDE (UNII: SOI2LOH54Z)
SELENIUM (UNII: H6241UJ22B)

Product Characteristics
Color	white	Score	score with uneven pieces
Shape	OVAL	Size	12mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55259-5001-1	1 in 1 PACKAGE	04/20/2019
1		120 in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/18/2015

Labeler - APEXEL CO., LTD. (687287979)

Registrant - APEXEL CO., LTD. (687287979)

Establishment
Name	Address	ID/FEI	Business Operations
APEXEL CO., LTD.		687287979	manufacture(55259-5001)