Unda 23

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 02:18:27

Label at a glance#

ProductUnda 23
Active ingredientSTRYCHNOS NUX-VOMICA SEED, QUERCUS ROBUR TWIG BARK, EQUISETUM ARVENSE BRANCH, HYPERICUM PERFORATUM, POTENTILLA ERECTA ROOT
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Each drop contains:
Equisetum arvense (Common horsetail) Stem 5X
Hypericum perforatum (St. John's Wort) Whole Plant 5X
Nux vomica (Poison nut) Seed 6X (< 2.7 x 10-6 % alkaloids, calculated)
Quercus robur (Common oak) Bark 6X
Tormentilla (Bloodwort) Underground Parts 6X

OTC - PURPOSE SECTION

Uses
For the temporary relief of symptoms associated with
occasional incontinence
minor urinary discomfort

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 - STOP USE SECTION

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

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.

OVERDOSAGE SECTION

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

INACTIVE INGREDIENT SECTION

Inactive ingredients
Ethanol (beet), purified water

OTHER SAFETY INFORMATION

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

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
occasional incontinence
minor urinary discomfort

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

62106-112262106-1122

NDC 62106-1122-8

UNDA

numbered compounds

UNDA 23

Homeopathic Preparation

For the temporary relief of symptoms associated

with occasional incontinence and minor urinary discomfort.

Contains 31% Alcohol
0.7 fl oz (20 mL)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62106-1122-8Unda 2320 mL in 1 BOTTLE, GLASSLIQUID204
62106-1122-8Unda 231 in 1 CARTONLIQUID14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62106-1122UNDA 23 (EQUISETUM ARVENSE, HYPERICUM PERFORATUM, NUX VOMICA, QUERCUS ROBUR, TORMENTILLA,) LIQUID [SEROYAL USA]4Current NDC, Legacy NDC, 2 package rows20221110_26e6ed42-2103-5968-e054-00144ff88e88.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62106-112262106-1122-8

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
Unda 23EQUISETUM ARVENSE, HYPERICUM PERFORATUM, NUX VOMICA, QUERCUS ROBUR, TORMENTILLA,Seroyal USA26e6ed42-2103-5968-e054-00144ff88e882022-11-09WarningsExact identifier
ndc (package): 62106-1122-8
ndc (product): 62106-1122
ndc11 (package): 62106112208
spl id: ed1057a6-61b8-96ab-e053-2a95a90ae050
spl set id: 26e6ed42-2103-5968-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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