ALUMIZEN

Manufacturer
Natural Creations, Inc. | OHM Pharma, Inc
Effective date
2025-11-13
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:35:10

Label at a glance#

ProductALUMIZEN
Active ingredientGARLIC, AVENA SATIVA FLOWERING TOP, BERBERIS VULGARIS ROOT BARK, ARCTIUM LAPPA ROOT, PHYTOLACCA AMERICANA ROOT, SOLIDAGO VIRGAUREA FLOWERING TOP, ALUMINUM OXIDE, SILVER NITRATE, BARIUM CARBONATE, BERYLLIUM, CADMIUM, copper, HYDROFLUORIC ACID, INDIUM, IODINE, LITHIUM CARBONATE, MERCURIUS SOLUBILIS, NICKEL CARBONATE HYDROXIDE TETRAHYDRATE, NITROUS OXIDE, lead, SELENIUM, STRONTIUM CARBONATE, TITANIUM, ARSENIC TRIOXIDE, SODIUM CHLORIDE, STRYCHNOS NUX-VOMICA SEED
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS: Allium Sat 6X, Avena 6X, Berber Vulg 6X, Lappa 6X, Phytolacca 6X, Solidago 6X, Alumina 6C, 12C, Arg Nit 6C, 12C, Baryta Carb 6C, 12C, Beryllium 6C, 12C, Cadmium Met 6C, 12C, Cuprum Met 6C, 12C, Fluoricum Acidum 6C, 12C, Indium 6C, 12C, Iodium 6C, 12C, Lithium Carb 6C, 12C, Merc Solub 6C, 12C, Niccolum Carb 6C, 12C, Nitrogenum Oxygenatum 6C, 12C, Plumb Met 6C, 12C, Selenium 6C, 12C, Strontium Carb 6C, 12C, Titanium 6C, 12C, Arsenicum Alb 12C, Nat Mur 12C, Nux Vom 12C.

OTC - PURPOSE SECTION

USES: Temporarily relieves weakness and fatigue.**

INDICATIONS & USAGE SECTION

USES: Temporarily relieves weakness and fatigue.**

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS: Adults & children above 12 years: 10 drops orally 3 times daily, or as directed by a health care professional.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.

WARNINGS SECTION

WARNINGS:

* Consult a physician for use in children under 12 years of age.

* IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use.

* KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.

* Do not use if TAMPER EVIDENT seal is broken or missing.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: Ethyl Alcohol USP, Purified Water.

OTC - QUESTIONS SECTION

QUESTIONS & COMMENTS?

Natural Creations, Inc. / Woodbine, IA 51579 / 712-647-1600

REFERENCES SECTION

** Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 43406-0641-1

ALUMIZEN

HOMEOPATHIC

1 fl oz (30 mL) / 20% Alcohol

 UPC: 877730004796

image descriptionimage description

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130877730004796GTIN-13: 0877730004796
EAN-13: 0877730004796
GTIN-12: 877730004796
UPC-A: 877730004796
GTIN storage (14 digits): 00877730004796
ALUMIZEN.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
86fffa7b-d382-4771-a253-25cccb64b590Product name320251124
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FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43406-0641-12022-02-17C16284748780-1d6a99b39-8635-a426-e053-dadaa90af4c2ALUMIZEN
43406-0641-12022-01-28C16284748780-1d6a99b39-8635-a426-e053-dadaa90af4c2ALUMIZEN

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43406-0641-1ALUMIZEN30 mL in 1 BOTTLE, DROPPERLIQUID305

Products#

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

DailyMed product names page 1 of 1 · 38 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43406-064143406-0641-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 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
ALUMIZENGARLIC, AVENA SATIVA FLOWERING TOP, BERBERIS VULGARIS ROOT BARK, ARCTIUM LAPPA ROOT, PHYTOLACCA AMERICANA ROOT, SOLIDAGO VIRGAUREA FLOWERING TOP, ALUMINUM OXIDE, SILVER NITRATE, BARIUM CARBONATE, BERYLLIUM, CADMIUM, COPPER, HYDROFLUORIC ACID, INDIUM, IODINE, LITHIUM CARBONATE, MERCURIUS SOLUBILIS, NICKEL CARBONATE HYDROXIDE TETRAHYDRATE, NITROUS OXIDE, LEAD, SELENIUM, STRONTIUM CARBONATE, TITANIUM, ARSENIC TRIOXIDE, SODIUM CHLORIDE, STRYCHNOS NUX-VOMICA SEED.Natural Creations, Inc.4760ab09-1141-4944-b840-804ae6d86d2d2025-11-13WarningsExact identifier
ndc (package): 43406-0641-1
ndc (product): 43406-0641
ndc11 (package): 43406064101
spl id: 35cd537e-4029-4893-aa90-ae20b7941d0d
spl set id: 4760ab09-1141-4944-b840-804ae6d86d2d

Reported adverse events (FAERS/openFDA)#

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