FDA.reportPublic FDA data

Natural Liquid Mineral Supplement

Manufacturer
Herbal Science International Inc
Effective date
2015-08-20
Label type
HUMAN OTC DRUG LABEL
Version
3150
Source
full-release
Hydrated at
2026-05-31 22:43:22

Label at a glance#

ProductNatural Liquid Mineral Supplement
Active ingredientZINC, CALCIUM, MAGNESIUM, MANGANESE, CHROMIUM
Label structure10 sections

Indications and uses

Temporary relief of symptoms related to mineral - imbalance in the body including fatigue, immunity, liver, dehydration, nervousness and cramping pains.

Storage and handling

Store at room temperature and keep away from direct sunlight. Self Life: 5 Years from the date of manufacture.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Zinc  2 mg

Calcium  40 mg

Magnesium  350 mg

Manganese  20 mg

Chromium  0.8 mg

Purpose

OTC - PURPOSE SECTION

Zinc                  supports immunity

Calcium            supports bone health

Magnesium      supports memory

Manganese      supports anti aging

Chromium        supports heart health

Indications and Usage

INDICATIONS & USAGE SECTION

Temporary relief of symptoms related to mineral - imbalance in the body including fatigue, immunity, liver, dehydration, nervousness and cramping pains.

Use

INSTRUCTIONS FOR USE SECTION

For ages 12 and up, take 10 - 30 ml and dilute in 500 - 1500 ml pure water daily. For ages between 12 and 2, take 5 - 10 ml and dilute in 500 ml pure water daily, and for ages under 2, take 2 - 5 ml and dilute in 100 ml pure water daily.

Warnings

USER SAFETY WARNINGS SECTION

If pregnant, breast-feeding, or have any allergic reaction to trace minerals, any chronic or recurring symptoms; or illness, consult a health professional before use.

Keep Out of Reach of Children.

WARNINGS SECTION

Keep out of reach of children.

Storage

STORAGE AND HANDLING SECTION

Store at room temperature and keep away from direct sunlight.

Self Life: 5 Years from the date of manufacture.

Questions or Comments?

OTC - QUESTIONS SECTION

Manufactured by Herbal Science International Inc.

                           205 Russell Street, City of Industry, CA 91748

Manufactured Exclusively For

           and

Exported Only by Zhientang Inc

                           19811 Colima Road, #330, Walnut, CA 91789

                           (626)417-3887

Inactive Ingredient

INACTIVE INGREDIENT SECTION

SODIUM, STRONTIUM, SILVER, COPPER, CADMIUM, LITHIUM, COBALT, IRON, WATER

Drug Facts

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CALCIUM Pharmacologic Class Indexing3Indexing - Pharmacologic Class20230427
CHROMIUM Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

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
69775-001-012020-01-31C16284748780-19d75b9cf-f5c3-f424-e053-dadaa90a57ceHerbal Science International Inc

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69775-001-01Natural Liquid Mineral Supplement200 mL in 1 BOTTLE, PLASTICLIQUID2003150

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69775-001NATURAL LIQUID MINERAL SUPPLEMENT (IRON, MANGANESE, CHROMIUM, MAGNESIUM) LIQUID [HERBAL SCIENCE INTERNATIONAL INC]31501 package rows20150821_52fd715b-5a48-46ef-95f7-d1d6b7556414.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CALCIUMACTIVE INGREDIENTSY7Q814VUP3150
CHROMIUMACTIVE INGREDIENT0R0008Q3JB3150
MAGNESIUMACTIVE INGREDIENTI38ZP9992A3150
MANGANESEACTIVE INGREDIENT42Z2K6ZL8P3150
ZINCACTIVE INGREDIENTJ41CSQ7QDS3150
CALCIUMACTIVE MOIETYSY7Q814VUP3150
CHROMIUMACTIVE MOIETY0R0008Q3JB3150
MAGNESIUMACTIVE MOIETYI38ZP9992A3150
MANGANESEACTIVE MOIETY42Z2K6ZL8P3150
ZINCACTIVE MOIETYJ41CSQ7QDS3150
CADMIUMINACTIVE INGREDIENT00BH33GNGH3150
COBALTINACTIVE INGREDIENT3G0H8C93623150
COPPERINACTIVE INGREDIENT789U1901C53150
IRONINACTIVE INGREDIENTE1UOL152H73150
LITHIUMINACTIVE INGREDIENT9FN79X2M3F3150
SILVERINACTIVE INGREDIENT3M4G523W1G3150
SODIUMINACTIVE INGREDIENT9NEZ333N273150
STRONTIUMINACTIVE INGREDIENTYZS2RPE8LE3150
WATERINACTIVE INGREDIENT059QF0KO0R3150

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69775-00169775-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
ZINCJ41CSQ7QDSACTIB
CALCIUMSY7Q814VUPACTIB
MAGNESIUMI38ZP9992AACTIB
MANGANESE42Z2K6ZL8PACTIB
CHROMIUM0R0008Q3JBACTIB
SODIUM9NEZ333N27IACT
STRONTIUMYZS2RPE8LEIACT
SILVER3M4G523W1GIACT
COPPER789U1901C5IACT
CADMIUM00BH33GNGHIACT
LITHIUM9FN79X2M3FIACT
COBALT3G0H8C9362IACT
IRONE1UOL152H7IACT
WATER059QF0KO0RIACT

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 · 1 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
IRONIRONE1UOL152H7TABLET, EXTENDED RELEASE / ORAL5 mgExact 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
12b45654-ca77-4a2a-aa0c-2902d6c0a54c52fd715b-5a48-46ef-95f7-d1d6b75564142015-08-20WarningsExact identifier
spl id: 12b45654-ca77-4a2a-aa0c-2902d6c0a54c
spl set id: 52fd715b-5a48-46ef-95f7-d1d6b7556414

Reported adverse events (FAERS/openFDA)#

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