FDA.reportPublic FDA data

ALUMINA

Manufacturer
STANDARD HOMEOPATHIC COMPANY
Effective date
2021-10-14
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:32:22

Label at a glance#

ProductALUMINA
Active ingredientALUMINUM OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Made according to the Homeopathic Pharmacopoeia of the United States since 1903.

Warnings

WARNINGS SECTION

SPL UNCLASSIFIED SECTION

Do not use if cap band is missing or broken.

SPL UNCLASSIFIED SECTION

If you are pregnant or nursing, consult a licensed health care professional before using this product.

SPL UNCLASSIFIED SECTION

If symptoms persist for 7 days or worsen, contact a licensed practitioner.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medicines out of the reach of children.

SPL UNCLASSIFIED SECTION

To be used according to label indications and/or standard homeopathic indications.

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS:ADULTS: Dissolve 4 tablets under tongue 4 times a day.

CHILDREN: Consult a health care professional.

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

DRY EYES OR DRY THROAT

INACTIVE INGREDIENT SECTION

In a base of Acacia Gum and Lactose N.F.

OTC - QUESTIONS SECTION

800-624-9659

OTC - ACTIVE INGREDIENT SECTION

ALUMINA 30X

Principal Display Panel - 250 Tablet Bottle

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Standard

Homeopathic

Made in the USA Since 1903

NDC # 0360-0017-01

Homeopathic Medicine

ALUMINA

30X

DRY EYES OR DRY THROAT*

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

250 TABLETS

labellabel

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0360-00170360-0017-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
ACACIA5C5403N26OIACT
LACTOSE MONOHYDRATEEWQ57Q8I5XIACT
ALUMINUM OXIDELMI26O6933ACTIB

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
ce513f61-096d-82a1-e053-2a95a90ab5a64a2c3c98-4e38-1c9b-e054-00144ff88e882021-10-14WarningsExact identifier
spl id: ce513f61-096d-82a1-e053-2a95a90ab5a6
spl set id: 4a2c3c98-4e38-1c9b-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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