FDA.reportPublic FDA data

Unda 1

Manufacturer
Seroyal USA | SAN’UP
Effective date
2022-11-07
Label type
HUMAN OTC DRUG LABEL
Version
20
Source
full-release
Hydrated at
2026-06-01 02:18:22

Label at a glance#

ProductUnda 1
Active ingredientACHILLEA MILLEFOLIUM, ARCTOSTAPHYLOS UVA-URSI LEAF, VALERIAN, ANGELICA ARCHANGELICA ROOT, EQUISETUM ARVENSE TOP, LYCOPODIUM CLAVATUM SPORE, LARIX DECIDUA RESIN, SILVER
Label structure9 sections

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

Uses
For the temporary relief of symptoms associated with
indigestion
fatigue following meals
occasional headaches

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 - ACTIVE INGREDIENT SECTION

Active ingredients
Each drop contains:
Angelica archangelica (European angelica) Root 4X
Argentum metallicum (Silver) 12X
Equisetum arvense (Common horsetail) Stem 4X
Lycopodium clavatum (Clubmoss) Spore 4X
Millefolium (Yarrow) Aerial Parts 4X
Resina larcis (Larch turnpentine) Balsam 5X
Uva-ursi (Bearberry) Leaf 4X
Valeriana officinalis (Valerian) Root 4X

INACTIVE INGREDIENT SECTION

Inactive ingredients
Ethanol (beet), purified water

INDICATIONS & USAGE SECTION

Uses
For the temporary relief of symptoms associated with
indigestion
fatigue following meals
occasional headaches

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.

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.

OTC - STOP USE SECTION

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

OTHER SAFETY INFORMATION

Do not use if seal is missing or broken.

Store in a cool dry place.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

62106-1100-862106-1100-8

NDC 62106-1100-8

UNDA

numbered compounds

UNDA 1

Homeopathic Preparation

For the temporary
relief of symptoms associated with
indigestion, fatigue following meals

and occasional headaches.

Contains 31% Alcohol

0.7 fl oz (20 ml)

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62106-1100-8Unda 11 in 1 CARTONLIQUID120
62106-1100-8Unda 120 mL in 1 BOTTLELIQUID2020

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62106-1100UNDA 1 (ACHILLEA MILLEFOLIUM) LIQUID [SEROYAL USA]20Current NDC, Legacy NDC, 2 package rows20221108_03c2e772-efa0-5a69-e054-00144ff88e88.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ACHILLEA MILLEFOLIUMACTIVE INGREDIENT2FXJ6SW4PK14
ANGELICA ARCHANGELICA ROOTACTIVE INGREDIENTDTN01M69SN14
ARCTOSTAPHYLOS UVA-URSI LEAFACTIVE INGREDIENT3M5V3D1X3614
EQUISETUM ARVENSE TOPACTIVE INGREDIENT1DP6Y6B65Z14
LARIX DECIDUA RESINACTIVE INGREDIENTAD8LJ73GQF14
LYCOPODIUM CLAVATUM SPOREACTIVE INGREDIENTC88X29Y47914
SILVERACTIVE INGREDIENT3M4G523W1G14
VALERIANACTIVE INGREDIENTJWF5YAW3QW14
ACHILLEA MILLEFOLIUMACTIVE MOIETY2FXJ6SW4PK14
ANGELICA ARCHANGELICA ROOTACTIVE MOIETYDTN01M69SN14
ARCTOSTAPHYLOS UVA-URSI LEAFACTIVE MOIETY3M5V3D1X3614
EQUISETUM ARVENSE TOPACTIVE MOIETY1DP6Y6B65Z14
LARIX DECIDUA RESINACTIVE MOIETYAD8LJ73GQF14
LYCOPODIUM CLAVATUM SPOREACTIVE MOIETYC88X29Y47914
SILVERACTIVE MOIETY3M4G523W1G14
VALERIANACTIVE MOIETYJWF5YAW3QW14
ALCOHOLINACTIVE INGREDIENT3K9958V90M14

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62106-110062106-1100-8

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ACHILLEA MILLEFOLIUM2FXJ6SW4PKACTIB
ARCTOSTAPHYLOS UVA-URSI LEAF3M5V3D1X36ACTIB
VALERIANJWF5YAW3QWACTIB
ANGELICA ARCHANGELICA ROOTDTN01M69SNACTIB
ALCOHOL3K9958V90MIACT
EQUISETUM ARVENSE TOP1DP6Y6B65ZACTIB
LYCOPODIUM CLAVATUM SPOREC88X29Y479ACTIB
LARIX DECIDUA RESINAD8LJ73GQFACTIB
SILVER3M4G523W1GACTIB

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 1ACHILLEA MILLEFOLIUMSeroyal USA03c2e772-efa0-5a69-e054-00144ff88e882022-11-07WarningsExact identifier
ndc (package): 62106-1100-8
ndc (product): 62106-1100
ndc11 (package): 62106110008
spl id: ece42ac2-e879-2756-e053-2995a90a55cb
spl set id: 03c2e772-efa0-5a69-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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