FDA.reportPublic FDA data

ENA Actimineral A

Manufacturer
Jinju Bio Food
Effective date
2013-06-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:35:49

Label at a glance#

ProductENA Actimineral A
Active ingredientCALCIUM
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

calcium


INACTIVE INGREDIENT SECTION

iron, zinc, magnesium, sodium, potassium, copper


OTC - PURPOSE SECTION

supplying various minerals to human body


OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out or reach of the children


INDICATIONS & USAGE SECTION

- It is thick alkaline solution of above pH12, so please dilute with mineral water when in use.
- Please dilute about 2ml~100ml similar with 1~5 lids of bottle in 1~2L and drink often.
- Mineral precipitate might be seen depending on storage state, so please shake and drink

WARNINGS SECTION

avoid contact with eyes



DOSAGE & ADMINISTRATION SECTION

for external use only


PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label
package label

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c599c4a0-705d-4ebb-ab1f-977af038f96aProduct name120251124
910c1bd7-67d1-44c7-ad4f-9445f827edccProduct name120230808

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58543-1001-12020-01-31C16284748780-19d75b9d0-3e0b-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58543-1001-1ENA Actimineral A1000 mL in 1 BOTTLELIQUID10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58543-1001ENA ACTIMINERAL A (CALCIUM) LIQUID [JINJU BIO FOOD]1Legacy NDC, 1 package rows20130629_f326c03b-6a7c-4fc7-941e-5dde096d6bad.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CALCIUMACTIVE INGREDIENTSY7Q814VUP1
CALCIUMACTIVE MOIETYSY7Q814VUP1
COPPERINACTIVE INGREDIENT789U1901C51
IRONINACTIVE INGREDIENTE1UOL152H71
MAGNESIUMINACTIVE INGREDIENTI38ZP9992A1
POTASSIUMINACTIVE INGREDIENTRWP5GA015D1
SODIUMINACTIVE INGREDIENT9NEZ333N271
ZINCINACTIVE INGREDIENTJ41CSQ7QDS1

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58543-100158543-1001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
CALCIUMSY7Q814VUPACTIB
IRONE1UOL152H7IACT
ZINCJ41CSQ7QDSIACT
MAGNESIUMI38ZP9992AIACT
POTASSIUMRWP5GA015DIACT
COPPER789U1901C5IACT
SODIUM9NEZ333N27IACT

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 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
IRONIRONE1UOL152H7TABLET, EXTENDED RELEASE / ORAL5 mgExact identifier — unii candidate
ZINCZINCJ41CSQ7QDSINJECTION / SUBCUTANEOUS0.02 %w/vExact identifier — unii candidate

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
7dfe8436-37a1-4f35-929d-5ed6d692b1aff326c03b-6a7c-4fc7-941e-5dde096d6bad2013-06-28WarningsExact identifier
spl id: 7dfe8436-37a1-4f35-929d-5ed6d692b1af
spl set id: f326c03b-6a7c-4fc7-941e-5dde096d6bad

Reported adverse events (FAERS/openFDA)#

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