UNDA 710

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 35
Active ingredientGOLD, CORALLIUM RUBRUM EXOSKELETON, CRATAEGUS FRUIT, GRINDELIA HIRSUTULA FLOWERING TOP, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, MENTHA PIPERITA, MYRTUS COMMUNIS TOP, LYCOPODIUM CLAVATUM SPORE, SOLANUM DULCAMARA TOP, CALENDULA OFFICINALIS FLOWERING TOP, APIS MELLIFERA
Label structure24 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Each drop contains:
Aurum metallicum (Gold) 12X
Corallium rubrum (Red coral) Exoskeleton 12X
Crataegus (Hawthorn) Fruit 4X
Grindelia Aerial Parts 4X
Hamamelis virginiana (Witch hazel) Bark 4X
Mentha piperita Aerial Parts 4X
Myrtus communis (Myrtle) Leafy Twigs 4X

OTC - PURPOSE SECTION

Uses
For the temporary relief of symptoms associated with cough.

WARNINGS SECTION

Warnings

Ask a doctor before use if you have
Persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema.
Cough that is accompanied by excessive phlegm (mucus) or fever.
Stop use and ask a doctor if
Cough persists for more than 1 week, tends to recur, or is accompanied by a fever, rash, or
persistent headache. A persistent cough may be a sign of a serious condition.
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.

OTC - STOP USE SECTION

Stop use and ask a doctor if
Cough persists for more than 1 week, tends to recur, or is accompanied by a fever, rash, or persistent headache. A persistent
cough may be a sign of a serious condition.
Symptoms persist or worsen.

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.
Contents may not fill package in order to accommodate required labeling. Please rely on stated quantity.

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 cough.

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:
Apis mellifica (Honeybee) Live Bees 4X
Aurum metallicum (Gold) 12X
Calendula officinalis (Marigold) Flowering Tops 4X
Dulcamara (Bittersweet) Shoots 4X
Lycopodium clavatum (Clubmoss) Spore 4X

OTC - PURPOSE SECTION

Uses
For the temporary relief of symptoms associated with common colds.

WARNINGS SECTION

Warning

Sore throat warning: Severe or persistent sore throat or sore throat accompanied

by high fever, headache, nausea and vomiting maybe serious.

Consult physician promptly.

Do not use more than 2 days or administer to children under 3 years of age unless directed by physician.

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 - DO NOT USE SECTION

Do not use more than 2 days or administer to children under 3 years of age unless directed by physician.

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

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 common colds.

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.

OTHER SAFETY INFORMATION

Other information
Do not use if seal is missing or broken.
Store in a cool, dry place.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

62106-113462106-1134

NDC 62106-1134-8

UNDA

numbered compounds

UNDA 35

Homeopathic Preparation

For the temporary relief of symptoms
associated with cough.

Contains 31% Alcohol
0.7 fl oz (20 mL)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

62106-1172-862106-1172-8

NDC 62106-1172-8

UNDA

numbered compounds

UNDA 710

Homeopathic Preparation

For the temporary relief of

symptoms associated with
common colds.

Contains 30% Alcohol
0.7 fl oz (20 ml)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62106-1134-8UNDA 351 in 1 CARTONLIQUID16
62106-1134-8UNDA 3520 mL in 1 BOTTLE, GLASSLIQUID206
62106-1172-8UNDA 7101 in 1 CARTONLIQUID16
62106-1172-8UNDA 71020 mL in 1 BOTTLE, GLASSLIQUID206

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62106-1134UNDA 35 (AURUM METALLICUM, CORALLIUM RUBRUM EXOSKELETON, CRATAEGUS, GRINDELIA, HAMAMELIS VIRGINIANA, MENTHA PIPERITA, MYRTUS COMMUNIS) LIQUID UNDA 710 (APIS MELLIFICA, CALENDULA OFFICINALIS, LYCOPODIUM CLAVATUM, DULCAMARA, AURUM METALLICUM) LIQUID [SEROYAL USA]6Current NDC, Legacy NDC, 2 package rows20221110_1f64baba-eb29-30c6-e054-00144ff8d46c.zip
62106-1172UNDA 35 (AURUM METALLICUM, CORALLIUM RUBRUM EXOSKELETON, CRATAEGUS, GRINDELIA, HAMAMELIS VIRGINIANA, MENTHA PIPERITA, MYRTUS COMMUNIS) LIQUID UNDA 710 (APIS MELLIFICA, CALENDULA OFFICINALIS, LYCOPODIUM CLAVATUM, DULCAMARA, AURUM METALLICUM) LIQUID [SEROYAL USA]6Current NDC, Legacy NDC, 2 package rows20221110_1f64baba-eb29-30c6-e054-00144ff8d46c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
APIS MELLIFERAACTIVE INGREDIENT7S82P3R43Z2
CALENDULA OFFICINALIS FLOWERING TOPACTIVE INGREDIENT18E7415PXQ2
CORALLIUM RUBRUM EXOSKELETONACTIVE INGREDIENT2CA71K0DLE2
CRATAEGUS FRUITACTIVE INGREDIENTQ21UUL21052
GOLDACTIVE INGREDIENT79Y1949PYO2
GRINDELIA HIRSUTULA FLOWERING TOPACTIVE INGREDIENTIDB0NAZ6AI2
HAMAMELIS VIRGINIANA ROOT BARK/STEM BARKACTIVE INGREDIENTT7S323PKJS2
LYCOPODIUM CLAVATUM SPOREACTIVE INGREDIENTC88X29Y4792
MENTHA PIPERITAACTIVE INGREDIENT79M2M2UDA92
MYRTUS COMMUNIS TOPACTIVE INGREDIENT367E55FXGW2
SOLANUM DULCAMARA TOPACTIVE INGREDIENTKPS1B1162N2
APIS MELLIFERAACTIVE MOIETY7S82P3R43Z2
CALENDULA OFFICINALIS FLOWERING TOPACTIVE MOIETY18E7415PXQ2
CORALLIUM RUBRUM EXOSKELETONACTIVE MOIETY2CA71K0DLE2
CRATAEGUS FRUITACTIVE MOIETYQ21UUL21052
GOLDACTIVE MOIETY79Y1949PYO2
GRINDELIA HIRSUTULA FLOWERING TOPACTIVE MOIETYIDB0NAZ6AI2
HAMAMELIS VIRGINIANA ROOT BARK/STEM BARKACTIVE MOIETYT7S323PKJS2
LYCOPODIUM CLAVATUM SPOREACTIVE MOIETYC88X29Y4792
MENTHA PIPERITAACTIVE MOIETY79M2M2UDA92
MYRTUS COMMUNIS TOPACTIVE MOIETY367E55FXGW2
SOLANUM DULCAMARA TOPACTIVE MOIETYKPS1B1162N2
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
62106-113462106-1134-8
62106-117262106-1172-8

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 35AURUM METALLICUM, CORALLIUM RUBRUM EXOSKELETON, CRATAEGUS, GRINDELIA, HAMAMELIS VIRGINIANA, MENTHA PIPERITA, MYRTUS COMMUNISSeroyal USA1f64baba-eb29-30c6-e054-00144ff8d46c2022-11-09WarningsExact identifier
ndc (package): 62106-1134-8
ndc (package): 62106-1172-8
ndc (product): 62106-1172
ndc (product): 62106-1134
ndc11 (package): 62106117208
ndc11 (package): 62106113408
spl id: ed10a243-116f-a82f-e053-2a95a90a0cf6
spl set id: 1f64baba-eb29-30c6-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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