AG-X

Manufacturer
APEXEL CO., LTD.
Effective date
2024-02-20
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:08:49

Label at a glance#

ProductAG-X
Active ingredientCALCIUM
Label structure8 sections

Indications and uses

for oral use only

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

calcium

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

magnesium, vitamin D, red ginseng powder

PURPOSE

OTC - PURPOSE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

WARNING

WARNINGS SECTION

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

DOSAGE & ADMINISTRATION SECTION

for oral use only

INDICATION & USAGE SECTION

INDICATIONS & USAGE SECTION

take two capsules once, two times a day

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Pharmacologic Classes#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55259-0007-12024-02-20C16284748780-11030e365-2748-111a-e063-dadaa90a10e2bdee5e24-645b-7fa0-e053-2995a90a7d25
55259-0007-12024-01-30C16284748780-11030e365-2748-111a-e063-dadaa90a10e2bdee5e24-645b-7fa0-e053-2995a90a7d25

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55259-0007-1AG-X120 in 1 BOTTLETABLET1203

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55259-0007AG-X (CALCIUM) TABLET [APEXEL CO., LTD.]3Current NDC, Legacy NDC, 1 package rows20240221_bdee5e24-645b-7fa0-e053-2995a90a7d25.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55259-000755259-0007-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

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
AG-XCALCIUMAPEXEL CO., LTD.bdee5e24-645b-7fa0-e053-2995a90a7d252024-02-20WarningsExact identifier
ndc (package): 55259-0007-1
ndc (product): 55259-0007
ndc11 (package): 55259000701
spl id: 11cc283a-fe2c-f101-e063-6294a90ad2d4
spl set id: bdee5e24-645b-7fa0-e053-2995a90a7d25

Reported adverse events (FAERS/openFDA)#

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