UNDA 31

Manufacturer
Seroyal USA | SAN’UP
Effective date
2022-11-09
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:18:28

Label at a glance#

ProductUNDA 31
Active ingredientSILVER, CINNAMOMUM CAMPHORA WHOLE, CENTAUREA BENEDICTA, JUNIPERUS COMMUNIS WHOLE, ARCTIUM LAPPA ROOT, ROBINIA PSEUDOACACIA BARK
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Each drop contains:
Argentum metallicum (Silver) 12X
Camphora (Camphor from Cinnamomum camphora) 12X
Carduus benedictus (Blessed Thistle) Aerial Parts 4X
Juniperus communis (Common juniper) Berry 4X
Lappa major (Great Burdock) Root 4X
Robinia pseudoacacia (Black locust) Bark 4X

OTC - PURPOSE SECTION

Uses
For the temporary relief of symptoms
associated with mild stomach 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 - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

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

DOSAGE & ADMINISTRATION SECTION

Directions
Adults and adolescents (12 years and older)

Take 5 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 stomach upset.

Directions
Adults and adolescents (12 years and older): Take 5 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

62106-113062106-1130

NDC 62106-1130-8

UNDA

numbered compounds

UNDA 31

Homeopathic Preparation

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

Contains 31% Alcohol
0.7 fl oz (20 ml)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62106-1130-8UNDA 3120 mL in 1 BOTTLE, GLASSLIQUID204
62106-1130-8UNDA 311 in 1 CARTONLIQUID14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62106-1130UNDA 31 (ARGENTUM METALLICUM, CAMPHORA, CARDUUS BENEDICTUS, JUNIPERUS COMMUNIS, LAPPA MAJOR, ROBINIA PSEUDOACACIA) LIQUID [SEROYAL USA]4Current NDC, Legacy NDC, 2 package rows20221110_2f0cd4d0-55a9-64b4-e054-00144ff8d46c.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
62106-113062106-1130-8

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML · Source PDF

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
UNDA 31ARGENTUM METALLICUM, CAMPHORA, CARDUUS BENEDICTUS, JUNIPERUS COMMUNIS, LAPPA MAJOR, ROBINIA PSEUDOACACIASeroyal USA2f0cd4d0-55a9-64b4-e054-00144ff8d46c2022-11-09WarningsExact identifier
ndc (package): 62106-1130-8
ndc (product): 62106-1130
ndc11 (package): 62106113008
spl id: ed107ed6-cf0b-1d5a-e053-2a95a90af33b
spl set id: 2f0cd4d0-55a9-64b4-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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