GELFOS-M

Manufacturer
I World Pharmaceutical Co., Ltd.
Effective date
2025-02-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 20:41:17

Label at a glance#

ProductGELFOS-M
Active ingredientALUMINUM PHOSPHATE, MAGNESIUM HYDROXIDE, DIMETHICONE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Aluminum Phosphate, Colloidal

Magnesium Hydroxide

Simethicone

OTC - PURPOSE SECTION

■ sour stomach ■ acid indigestion ■ upset stomach associated with these

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INDICATIONS & USAGE SECTION

■ take 2-3 envelops as symptoms accur, as directed by a doctor

WARNINGS SECTION

Warnings

Ask a doctor before use if you have taking a prescription drug. Antacids may interact with certain prescription drugs

When using this product

■ Do not take more than 4 envelop in 24 hours

■ Do not use the maximum dosage for more than 2 weeks

INACTIVE INGREDIENT SECTION

water, sugar, agar, pectin, essence of orange, calcium

DOSAGE & ADMINISTRATION SECTION

For oral use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73442-0003-12025-02-13C16284748780-12cef2736-5bfb-d83d-e063-dadaa90ab31f96e0edc5-2512-b9e2-e053-2a95a90a266c
73442-0003-12025-01-30C16284748780-12cef2736-5bfb-d83d-e063-dadaa90ab31f96e0edc5-2512-b9e2-e053-2a95a90a266c

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73442-0003GELFOS-M (ALUMINUM PHOSPHATE, COLLOIDAL, MAGNESIUM HYDROXIDE, SIMETHICONE) LIQUID [I WORLD PHARMACEUTICAL CO., LTD.]2Legacy NDC20250216_96e0edc5-2512-b9e2-e053-2a95a90a266c.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73442-000373442-0003-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
368fd898-d40f-8807-e063-6294a90ac7a796e0edc5-2512-b9e2-e053-2a95a90a266c2025-06-02WarningsExact identifier
spl set id: 96e0edc5-2512-b9e2-e053-2a95a90a266c

Reported adverse events (FAERS/openFDA)#

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