UNDA 38

Manufacturer
Seroyal USA | SAN’UP
Effective date
2022-11-09
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 02:18:26

Label at a glance#

ProductUNDA 29
Active ingredientLAMIUM ALBUM, WORMWOOD, ONION, SILVER, BETULA PENDULA WOOD, SAGE, ALUMINUM, INULA HELENIUM ROOT, SARSAPARILLA, CORN SILK, VALERIAN
Label structure24 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Each drop contains:
Absinthium (Common wormwood) Aerial Parts 4X
Allium cepa (Onion) Bulb 4X
Argentum metallicum (Silver) 12X
Betula pendula Sap 4X
Lamium album (Dead nettle) Flowering Tops 4X
Salvia officinalis (Garden sage) Leaf 4X

OTC - PURPOSE SECTION

Uses

For the temporary relief of mild joint and muscle aches.

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 mild joint and muscle aches.

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.

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Each drop contains equal parts of:

Aluminium metallicum (Aluminum) 12X
Argentum metallicum (Silver) 12X
Inula helenium (Elecampane) Root 4X
Sarsaparilla Root 4X
Stigmata maidis (Maize) Style and Stigma 4X
Valeriana officinalis (Valerian) Root 4X

OTC - PURPOSE SECTION

Uses
For the relief of symptoms associated with
minor difficulties in urination.

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 relief of symptoms associated with
minor difficulties in urination.

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

62106-112862106-1128

NDC 62106-1128-8

UNDA
numbered compounds
UNDA 29
Homeopathic Preparation

For the temporary relief of mild

joint and muscle aches.
Contains 31% Alcohol
0.7 fl oz (20 ml)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

62106-113762106-1137

NDC 62106-1137-8

UNDA
numbered compounds
UNDA 38
Homeopathic Preparation

For the temporary relief of symptoms
associated with minor difficulties in urination.
Contains 31% Alcohol
0.7 fl oz (20 mL)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62106-1128-8UNDA 291 in 1 CARTONLIQUID16
62106-1128-8UNDA 2920 mL in 1 BOTTLE, GLASSLIQUID206
62106-1137-8UNDA 381 in 1 CARTONLIQUID16
62106-1137-8UNDA 3820 mL in 1 BOTTLE, GLASSLIQUID206

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62106-1128UNDA 29 (ABSINTHIUM, ALLIUM CEPA, ARGENTUM METALLICUM, BETULA PENDULA SAP, LAMIUM ALBUM, SALVIA OFFICINALIS) LIQUID UNDA 38 (ALUMINIUM METALLICUM, ARGENTUM METALLICUM, INULA HELENIUM, SARSAPARILLA, STIGMATA MAIDIS, VALERIANA OFFICINALIS) LIQUID [SEROYAL USA]6Current NDC, Legacy NDC, 2 package rows20221110_20484d33-4389-1a85-e054-00144ff88e88.zip
62106-1137UNDA 29 (ABSINTHIUM, ALLIUM CEPA, ARGENTUM METALLICUM, BETULA PENDULA SAP, LAMIUM ALBUM, SALVIA OFFICINALIS) LIQUID UNDA 38 (ALUMINIUM METALLICUM, ARGENTUM METALLICUM, INULA HELENIUM, SARSAPARILLA, STIGMATA MAIDIS, VALERIANA OFFICINALIS) LIQUID [SEROYAL USA]6Current NDC, Legacy NDC, 2 package rows20221110_20484d33-4389-1a85-e054-00144ff88e88.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALUMINUMACTIVE INGREDIENTCPD4NFA9032
BETULA PENDULA WOODACTIVE INGREDIENT568ZVX88G62
CORN SILKACTIVE INGREDIENT7D3VB244UX2
INULA HELENIUM ROOTACTIVE INGREDIENTE55SMD6DA82
LAMIUM ALBUMACTIVE INGREDIENT046Y1357I62
ONIONACTIVE INGREDIENT492225Q21H2
SAGEACTIVE INGREDIENT065C5D077J2
SARSAPARILLAACTIVE INGREDIENT2H1576D5WG2
SILVERACTIVE INGREDIENT3M4G523W1G2
VALERIANACTIVE INGREDIENTJWF5YAW3QW2
WORMWOODACTIVE INGREDIENTF84709P2XV2
ALUMINUMACTIVE MOIETYCPD4NFA9032
BETULA PENDULA WOODACTIVE MOIETY568ZVX88G62
CORN SILKACTIVE MOIETY7D3VB244UX2
INULA HELENIUM ROOTACTIVE MOIETYE55SMD6DA82
LAMIUM ALBUMACTIVE MOIETY046Y1357I62
ONIONACTIVE MOIETY492225Q21H2
SAGEACTIVE MOIETY065C5D077J2
SARSAPARILLAACTIVE MOIETY2H1576D5WG2
SILVERACTIVE MOIETY3M4G523W1G2
VALERIANACTIVE MOIETYJWF5YAW3QW2
WORMWOODACTIVE MOIETYF84709P2XV2
ALCOHOLINACTIVE INGREDIENT3K9958V90M2
WATERINACTIVE INGREDIENT059QF0KO0R2

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62106-112862106-1128-8
62106-113762106-1137-8

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 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 · 4 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
4 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 29ABSINTHIUM, ALLIUM CEPA, ARGENTUM METALLICUM, BETULA PENDULA SAP, LAMIUM ALBUM, SALVIA OFFICINALISSeroyal USA20484d33-4389-1a85-e054-00144ff88e882022-11-09WarningsExact identifier
ndc (package): 62106-1128-8
ndc (package): 62106-1137-8
ndc (product): 62106-1128
ndc (product): 62106-1137
ndc11 (package): 62106112808
ndc11 (package): 62106113708
spl id: ed107ed6-cf0a-1d5a-e053-2a95a90af33b
spl set id: 20484d33-4389-1a85-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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