UNDA 243

Manufacturer
Seroyal USA | SAN’UP
Effective date
2022-11-08
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 02:18:23

Label at a glance#

ProductUNDA 10
Active ingredientSILVER, EQUISETUM ARVENSE BRANCH, JUNIPER BERRY, WORMWOOD, ACHILLEA MILLEFOLIUM, FRANGULA ALNUS BARK, PEUMUS BOLDUS LEAF, CHOLESTEROL, COMBRETUM MICRANTHUM LEAF, LYCOPODIUM CLAVATUM SPORE, PODOPHYLLUM PELTATUM ROOT
Label structure24 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Each drop contains:
Absinthium (Common wormwood) Aerial Parts 4X
Argentum metallicum (Silver) 12X
Equisetum arvense (Common horsetail) Stem 4X
Juniperus communis (Common juniper) Berry 4X
Millefolium (Yarrow) Aerial Parts 4X
Rhamnus frangula (Buckthorn) Bark 4X

OTC - PURPOSE SECTION

Uses

For the temporary relief of minor symptoms associated with occasional irregular menstrual cycles.

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 minor symptoms associated with occasional irregular menstrual cycles.

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:
Boldo Leaf 4X
Cholesterinum (Cholesterol) 12X
Combretum micranthum Leaf 4X
Lycopodium clavatum (Clubmoss) Spore 4X
Podophyllum peltatum (Mayapple) Underground Parts 4X

OTC - PURPOSE SECTION

Uses

For the temporary relief of symptoms associated with overindulgence in food and alcohol.

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.

INDICATIONS & USAGE SECTION

Uses

For the temporary relief of symptoms associated with overindulgence in food and alcohol.

Directions
Adults and adolescents (12 years and older): Take 5 drops three
times daily or as recommended by your healthcare practitioner.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

62106-110962106-1109

NDC 62106-1109-8

UNDA
numbered compounds
UNDA 10
Homeopathic Preparation

For the temporary relief of minor symptoms
associated with occasional irregular menstrual cycles.
Contains 31% Alcohol
0.7 fl oz (20 mL)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

62106-116262106-1162

NDC 62106-1162-8

UNDA
numbered compounds
UNDA 243
Homeopathic Preparation

For the temporary relief of symptoms
associated with overindulgence in
food and alcohol.
Contains 31% Alcohol
0.7 fl oz (20 mL)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62106-1109-8UNDA 101 in 1 CARTONLIQUID17
62106-1109-8UNDA 1020 mL in 1 BOTTLE, GLASSLIQUID207
62106-1162-8UNDA 24320 mL in 1 BOTTLE, GLASSLIQUID207
62106-1162-8UNDA 2431 in 1 CARTONLIQUID17

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62106-1109UNDA 10 (ABSINTHIUM, ARGENTUM METALLICUM, EQUISETUM ARVENSE, JUNIPERUS COMMUNIS, MILLEFOLIUM, RHAMNUS FRANGULA) LIQUID UNDA 243 (BOLDO LEAF, CHOLESTERINUM, COMBRETUM MICRANTHUM, LYCOPODIUM CLAVATUM, PODOPHYLLUM PELTATUM) LIQUID [SEROYAL USA]7Current NDC, Legacy NDC, 2 package rows20221109_20ea57db-ad94-2c1c-e054-00144ff88e88.zip
62106-1162UNDA 10 (ABSINTHIUM, ARGENTUM METALLICUM, EQUISETUM ARVENSE, JUNIPERUS COMMUNIS, MILLEFOLIUM, RHAMNUS FRANGULA) LIQUID UNDA 243 (BOLDO LEAF, CHOLESTERINUM, COMBRETUM MICRANTHUM, LYCOPODIUM CLAVATUM, PODOPHYLLUM PELTATUM) LIQUID [SEROYAL USA]7Current NDC, Legacy NDC, 2 package rows20221109_20ea57db-ad94-2c1c-e054-00144ff88e88.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ACHILLEA MILLEFOLIUMACTIVE INGREDIENT2FXJ6SW4PK3
CHOLESTEROLACTIVE INGREDIENT97C5T2UQ7J3
COMBRETUM MICRANTHUM LEAFACTIVE INGREDIENT8502S3Z5N13
EQUISETUM ARVENSE BRANCHACTIVE INGREDIENT1L0VKZ185E3
FRANGULA ALNUS BARKACTIVE INGREDIENTS2D77IH61R3
JUNIPER BERRYACTIVE INGREDIENTO84B5194RL3
LYCOPODIUM CLAVATUM SPOREACTIVE INGREDIENTC88X29Y4793
PEUMUS BOLDUS LEAFACTIVE INGREDIENTQ4EWM09M3O3
PODOPHYLLUM PELTATUM ROOTACTIVE INGREDIENT2S713A4VP33
SILVERACTIVE INGREDIENT3M4G523W1G3
WORMWOODACTIVE INGREDIENTF84709P2XV3
ACHILLEA MILLEFOLIUMACTIVE MOIETY2FXJ6SW4PK3
CHOLESTEROLACTIVE MOIETY97C5T2UQ7J3
COMBRETUM MICRANTHUM LEAFACTIVE MOIETY8502S3Z5N13
EQUISETUM ARVENSE BRANCHACTIVE MOIETY1L0VKZ185E3
FRANGULA ALNUS BARKACTIVE MOIETYS2D77IH61R3
JUNIPER BERRYACTIVE MOIETYO84B5194RL3
LYCOPODIUM CLAVATUM SPOREACTIVE MOIETYC88X29Y4793
PEUMUS BOLDUS LEAFACTIVE MOIETYQ4EWM09M3O3
PODOPHYLLUM PELTATUM ROOTACTIVE MOIETY2S713A4VP33
SILVERACTIVE MOIETY3M4G523W1G3
WORMWOODACTIVE MOIETYF84709P2XV3
ALCOHOLINACTIVE INGREDIENT3K9958V90M3
WATERINACTIVE INGREDIENT059QF0KO0R3

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
62106-110962106-1109-8
62106-116262106-1162-8

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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 10ABSINTHIUM, ARGENTUM METALLICUM, EQUISETUM ARVENSE, JUNIPERUS COMMUNIS, MILLEFOLIUM, RHAMNUS FRANGULASeroyal USA20ea57db-ad94-2c1c-e054-00144ff88e882022-11-08WarningsExact identifier
ndc (package): 62106-1109-8
ndc (package): 62106-1162-8
ndc (product): 62106-1109
ndc (product): 62106-1162
ndc11 (package): 62106110908
ndc11 (package): 62106116208
spl id: ecfa1477-78a8-d93d-e053-2995a90af9b8
spl set id: 20ea57db-ad94-2c1c-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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