Gastrunda

Manufacturer
Seroyal USA | SAN’UP
Effective date
2019-12-19
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:49:53

Label at a glance#

ProductGastrunda
Active ingredientCASHEW, SILVER NITRATE, MARSDENIA CONDURANGO BARK, ARSENIC TRIOXIDE, ATROPINE SULFATE, BISMUTH SUBNITRATE, HAMAMELIS VIRGINIANA BARK, GOLDENSEAL, POTASSIUM DICHROMATE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Each drop contains:
Anacardium orientale (Oriental cashew nut) Fruit 6X
Argentum nitricum (Silver nitrate) 4X
Arsenicum album (Arsenic trioxide) 6X
Atropinum sulfuricum (Atropine sulfate) 4X
Bismuthum subnitricum (Basic bismutnitrate) 8X
Condurango Bark 2X
Hamamelis virginiana (Witch hazel) Bark 2X
Hydrastis canadensis (Goldenseal) Underground Parts 4X
Kalium bichromicum (Potassium bichromate) 4X

OTC - PURPOSE SECTION

Uses

For the temporary relief of symptoms associated with mild digestive upset.

WARNINGS SECTION

Warnings
Stop use and ask a doctor if symptoms persist or worsen.

If pregnant or breastfeeding, ask a health professional before use.
Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTHER SAFETY INFORMATION

Other information
Do not use if seal is missing or broken.
Store in a cool, dry place.

INACTIVE INGREDIENT SECTION

Inactive ingredients
Ethanol (beet), purified water, glycerin

DOSAGE & ADMINISTRATION SECTION

Directions

To be taken ten minutes away from food.
Invert bottle and shake lightly allowing drops to fall directly under the tongue or into ¼ oz of water.
Hold contents for about 20 seconds and swallow.
To promote drop flow, invert bottle and shake before each use.
Dosage frequency may be increased up to six times daily depending on the severity of symptoms.

Adults and adolescents (12 years and older)

Take 10 drops three times daily or as recommended by your healthcare practitioner.

Children (under 12 years)

Take under the direction of your healthcare practitioner.

INDICATIONS & USAGE SECTION

Uses

For the temporary relief of symptoms associated with mild digestive upset.

Directions

To be taken ten minutes away from food.
Invert bottle and shake lightly allowing drops to fall directly under the tongue or into ¼ oz of water.
Hold contents for about 20 seconds and swallow.
To promote drop flow, invert bottle and shake before each use.
Dosage frequency may be increased up to six times daily depending on the severity of symptoms.

Adults and adolescents (12 years and older)

Take 10 drops three times daily or as recommended by your healthcare practitioner.

Children (under 12 years)

Take under the direction of your healthcare practitioner.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

62106-202562106-2025NDC 62106-2025-0

UNDA

plex

GASTRUNDA

Homeopathic Preparation

For the temporary relief of symptoms associated with mild digestive upset.

Contains 30% Alcohol
0.7 fl oz (20 mL)

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62106-202562106-2025-0

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
9a167396-0cb8-9a80-e053-2a95a90a3abc308c6667-c8ab-0a3d-e054-00144ff88e882019-12-19WarningsExact identifier
spl id: 9a167396-0cb8-9a80-e053-2a95a90a3abc
spl set id: 308c6667-c8ab-0a3d-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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