Unda 44

Manufacturer
Seroyal USA | SAN’UP
Effective date
2022-07-07
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:17:41

Label at a glance#

ProductUnda 44
Active ingredientGOLD, SILVER, JUNIPER BERRY, ARCTOSTAPHYLOS UVA-URSI LEAF, SOLANUM DULCAMARA STEM, CYTISUS SCOPARIUS FLOWERING TOP, CORN SILK, INULA HELENIUM ROOT
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients
Each drop contains:
Argentum metallicum (Silver) 12X
Aurum metallicum (Gold) 12X
Cytisus scoparius (Scotch broom) Aerial Parts 4X
Dulcamara (Bittersweet) Shoots 4X
Inula helenium (Elecampane) Root 4X
Juniperus communis (Common juniper) Berry 4X
Stigmata maidis (Maize) Style and Stigma 4X
Uva-ursi (Bearberry) Leaf 4X

OTC - PURPOSE SECTION

Uses
For the temporary relief of symptoms
associated with 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 - 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.

OTC - ASK DOCTOR SECTION

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

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 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

unda 44unda 44

NDC 62106-1143-8

UNDA

numbered compounds

UNDA 44

Homeopathic Preparation

For the temporary
relief of symptoms
associated with minor
urinary discomfort.

Contains 31% Alcohol
0.7 fl oz (20 ml)

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62106-1143-8Unda 4420 mL in 1 BOTTLE, GLASSLIQUID205
62106-1143-8Unda 441 in 1 BOXLIQUID15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62106-1143UNDA 44 (INULA HELENIUM ROOT, JUNIPERUS COMMUNIS BERRY, UVA-URSI LEAF, DULCAMARA STEM AND LEAF, CYTISUS SCOPARIUS AERIAL PARTS, STIGMATA MAIDIS STYLE AND STIGMA, ARGENTUM METALLICUM, AURUM METALLICUM) LIQUID [SEROYAL USA]5Current NDC, Legacy NDC, 2 package rows20220709_0a6df6e1-fe50-0f3e-e054-00144ff8d46c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ARCTOSTAPHYLOS UVA-URSI LEAFACTIVE INGREDIENT3M5V3D1X361
CORN SILKACTIVE INGREDIENT7D3VB244UX1
CYTISUS SCOPARIUS FLOWERING TOPACTIVE INGREDIENTXZC6H8R6661
GOLDACTIVE INGREDIENT79Y1949PYO1
INULA HELENIUM ROOTACTIVE INGREDIENTE55SMD6DA81
JUNIPER BERRYACTIVE INGREDIENTO84B5194RL1
SILVERACTIVE INGREDIENT3M4G523W1G1
SOLANUM DULCAMARA STEMACTIVE INGREDIENTIR986LE7DF1
ARCTOSTAPHYLOS UVA-URSI LEAFACTIVE MOIETY3M5V3D1X361
CORN SILKACTIVE MOIETY7D3VB244UX1
CYTISUS SCOPARIUS FLOWERING TOPACTIVE MOIETYXZC6H8R6661
GOLDACTIVE MOIETY79Y1949PYO1
INULA HELENIUM ROOTACTIVE MOIETYE55SMD6DA81
JUNIPER BERRYACTIVE MOIETYO84B5194RL1
SILVERACTIVE MOIETY3M4G523W1G1
SOLANUM DULCAMARA STEMACTIVE MOIETYIR986LE7DF1
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62106-114362106-1143-8

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates

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 44INULA HELENIUM ROOT, JUNIPERUS COMMUNIS BERRY, UVA-URSI LEAF, DULCAMARA STEM AND LEAF, CYTISUS SCOPARIUS AERIAL PARTS, STIGMATA MAIDIS STYLE AND STIGMA, ARGENTUM METALLICUM, AURUM METALLICUMSeroyal USA0a6df6e1-fe50-0f3e-e054-00144ff8d46c2022-07-07WarningsExact identifier
ndc (package): 62106-1143-8
ndc (product): 62106-1143
ndc11 (package): 62106114308
spl id: e33beb53-7971-929e-e053-2995a90a6fa0
spl set id: 0a6df6e1-fe50-0f3e-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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