FDA.reportPublic FDA data

7030 Calcium Premium

Manufacturer
Apexel Co., Ltd
Effective date
2015-02-01
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:41:34

Label at a glance#

Product7030 Calcium Premium
Active ingredientCALCIUM
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

calcium

INACTIVE INGREDIENT SECTION

magnesium, zinc oxide, selenium, germanium, iron, potassium, manganese

OTC - PURPOSE SECTION

- to prevent and cure the osteoporosis
- to prevent and cure the disease of cardiac and vascular
- to promote growth and healing

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

take two tablets everty time, two times a day with enough water

WARNINGS SECTION

• Do not use during pregnant, breast-feeding, or menstrual cycle
• Keep this product out of reach of children under 3 years old

DOSAGE & ADMINISTRATION SECTION

for oral use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package insert
package insert

DailyMed Pharmacologic Classes#

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

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codeck7057.wgiga.co.kr/calcium premium.jpg

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
55259-2001-12020-01-31C16284748780-19d75b9d0-2cda-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55259-2001-17030 Calcium Premium120 in 1 PACKAGECAPSULE1202

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55259-20017030 CALCIUM PREMIUM (CALCIUM) CAPSULE [APEXEL CO., LTD]2Legacy NDC, 1 package rows20150201_c09a73b6-d3dc-4e00-af45-a15722bde945.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CALCIUMACTIVE INGREDIENTSY7Q814VUP2
CALCIUMACTIVE MOIETYSY7Q814VUP2
GERMANIUMINACTIVE INGREDIENT00072J7XWS2
IRONINACTIVE INGREDIENTE1UOL152H72
MAGNESIUMINACTIVE INGREDIENTI38ZP9992A2
MANGANESEINACTIVE INGREDIENT42Z2K6ZL8P2
POTASSIUMINACTIVE INGREDIENTRWP5GA015D2
SELENIUMINACTIVE INGREDIENTH6241UJ22B2
ZINC OXIDEINACTIVE INGREDIENTSOI2LOH54Z2

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55259-200155259-2001-1

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
CALCIUMSY7Q814VUPACTIB
MAGNESIUMI38ZP9992AIACT
ZINC OXIDESOI2LOH54ZIACT
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 OXIDESOI2LOH54ZSOLUTION / RESPIRATORY (INHALATION)3.11 %w/vExact 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, SUSPENSION / SUBCUTANEOUSNAExact identifier — unii candidate
6 equally ranked IID candidates
ZINC OXIDEZINC OXIDESOI2LOH54ZINJECTION / SUBCUTANEOUS0.02 %w/vExact identifier — unii candidate
6 equally ranked IID candidates
IRONIRONE1UOL152H7TABLET, EXTENDED RELEASE / ORAL5 mgExact identifier — unii candidate
ZINC OXIDEZINC OXIDESOI2LOH54ZLOTION / TOPICAL16 %w/wExact identifier — unii candidate
6 equally ranked IID candidates
ZINC OXIDEZINC OXIDESOI2LOH54ZSUPPOSITORY / RECTAL375 mgExact 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
9d698942-f723-4adb-8095-760a7ad3fdd6c09a73b6-d3dc-4e00-af45-a15722bde9452015-02-01WarningsExact identifier
spl id: 9d698942-f723-4adb-8095-760a7ad3fdd6
spl set id: c09a73b6-d3dc-4e00-af45-a15722bde945

Reported adverse events (FAERS/openFDA)#

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