AG-X by APEXEL CO., LTD. AG-X- calcium tablet

AG-X by

Drug Labeling and Warnings

AG-X by is a Otc medication manufactured, distributed, or labeled by APEXEL CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

calcium

INACTIVE INGREDIENT

magnesium, vitamin D, red ginseng powder

PURPOSE

Treatment and prevention of osteoporosis

Growth and development

Treatment and prediction of cardiovascular disease due to calcification of blood

Attention deficit in children, depression, nervous symptoms, nervous stability to anxiety

Myalgia, Bone Pain, Arthritis, Dysmenorrhea Treatment

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

WARNING

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.

Any items past the expiration date or damaged in transit can be exchanged where you originally purchased the item.

consult your doctor if any abnormal symptoms occur

USES

for oral use only

INDICATION & USAGE SECTION

take two capsules once, two times a day

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AG-X 
calcium tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55259-8001
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CALCIUM (UNII: SY7Q814VUP) (CALCIUM - UNII:SY7Q814VUP)	CALCIUM	0.76

Inactive Ingredients
Ingredient Name	Strength
MAGNESIUM (UNII: I38ZP9992A)
PANAX GINSENG WHOLE (UNII: 9L5JEP7MES)
VITAMIN D (UNII: 9VU1KI44GP)

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: 55259-8001-1	120 in 1 BOTTLE; Type 0: Not a Combination Product	08/02/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		08/02/2019

Labeler - APEXEL CO., LTD. (687287979)

Registrant - APEXEL CO., LTD. (687287979)

Establishment
Name	Address	ID/FEI	Business Operations
APEXEL CO., LTD.		687287979	manufacture(55259-8001)