Unda 18

Manufacturer
Seroyal USA | SAN’UP
Effective date
2022-11-09
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:18:25

Label at a glance#

ProductUnda 18
Active ingredientANTIMONY, MARSDENIA CONDURANGO BARK, VIBURNUM PRUNIFOLIUM BARK, THUJA OCCIDENTALIS LEAFY TWIG, CINNAMOMUM CAMPHORA WHOLE, COPPER, LYCOPODIUM CLAVATUM SPORE, ALUMINUM
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients
Each drop contains:
Aluminium metallicum (Aluminum) 12X
Camphora (Camphor from Cinnamomum camphora) 9X
Condurango Bark 5X
Cuprum metallicum (Copper) 12X
Lycopodium clavatum (Clubmoss) Spore 5X
Stibium metallicum (Antimony) 12X
Thuja occidentalis (White cedar) Twig 5X
Viburnum prunifolium (Blackhaw) Bark 5X

OTC - PURPOSE SECTION

Uses
For the temporary relief of symptoms associated with
low energy
tiredness
overall exhaustion

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 - STOP USE SECTION

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

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
low energy
tiredness
overall exhaustion

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

62106-111762106-1117

NDC 62106-1117-8

UNDA

numbered compounds

UNDA 18

Homeopathic Preparation

For the temporary relief of symptoms associated with low energy, tiredness and overall exhaustion.

Contains 31% Alcohol
0.7 fl oz (20 ml)

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c599c4a0-705d-4ebb-ab1f-977af038f96aProduct name120251124
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62106-1117-8Unda 181 in 1 CARTONLIQUID15
62106-1117-8Unda 1820 mL in 1 BOTTLE, GLASSLIQUID205

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62106-1117UNDA 18 (CONDURANGO, LYCOPODIUM CLAVATUM, VIBURNUM PRUNIFOLIUM, THUJA OCCIDENTALIS, CAMPHORA, CUPRUM METALLICUM, ALUMINIUM METALLICUM, STIBIUM METALLICUM) LIQUID [SEROYAL USA]5Current NDC, Legacy NDC, 2 package rows20221110_0e71305f-4b5a-6d5a-e054-00144ff88e88.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALUMINUMACTIVE INGREDIENTCPD4NFA9031
ANTIMONYACTIVE INGREDIENT9IT35J3UV31
CINNAMOMUM CAMPHORA WHOLEACTIVE INGREDIENT0B27814T7X1
COPPERACTIVE INGREDIENT789U1901C51
LYCOPODIUM CLAVATUM SPOREACTIVE INGREDIENTC88X29Y4791
MARSDENIA CONDURANGO BARKACTIVE INGREDIENTR23QIR6YBA1
THUJA OCCIDENTALIS LEAFY TWIGACTIVE INGREDIENT1NT28V93971
VIBURNUM PRUNIFOLIUM BARKACTIVE INGREDIENTJ411UTU0HN1
ALUMINUMACTIVE MOIETYCPD4NFA9031
ANTIMONYACTIVE MOIETY9IT35J3UV31
CINNAMOMUM CAMPHORA WHOLEACTIVE MOIETY0B27814T7X1
COPPERACTIVE MOIETY789U1901C51
LYCOPODIUM CLAVATUM SPOREACTIVE MOIETYC88X29Y4791
MARSDENIA CONDURANGO BARKACTIVE MOIETYR23QIR6YBA1
THUJA OCCIDENTALIS LEAFY TWIGACTIVE MOIETY1NT28V93971
VIBURNUM PRUNIFOLIUM BARKACTIVE MOIETYJ411UTU0HN1
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
62106-111762106-1117-8

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 18CONDURANGO, LYCOPODIUM CLAVATUM, VIBURNUM PRUNIFOLIUM, THUJA OCCIDENTALIS, CAMPHORA, CUPRUM METALLICUM, ALUMINIUM METALLICUM, STIBIUM METALLICUMSeroyal USA0e71305f-4b5a-6d5a-e054-00144ff88e882022-11-09WarningsExact identifier
ndc (package): 62106-1117-8
ndc (product): 62106-1117
ndc11 (package): 62106111708
spl id: ed104a9f-7380-4f7b-e053-2995a90af948
spl set id: 0e71305f-4b5a-6d5a-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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