Unda 26

Manufacturer
Seroyal USA | SAN’UP
Effective date
2022-11-09
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:18:26

Label at a glance#

ProductUnda 26
Active ingredientMYRTUS COMMUNIS TOP, APIS MELLIFERA, SILVER
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients
Each drop contains:
Apis mellifica (Honeybee) Live Bees 4X
Argentum metallicum (Silver) 12X
Myrtus communis (Myrtle) Leafy Twigs 4X

OTC - PURPOSE SECTION

Uses
For the temporary relief of symptoms associated with minor inflammatory conditions of the gums and mouth.

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

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 symptoms associated with minor inflammatory conditions of the gums and mouth.

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

62106-112562106-1125

NDC 62106-1125-8

UNDA

numbered compounds

UNDA 26

Homeopathic Preparation

For the temporary relief of symptoms

associated with minor inflammatory

conditions of the gums and mouth.

Contains 31% Alcohol
0.7 fl oz (20 ml)

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62106-1125-8Unda 2620 mL in 1 BOTTLE, GLASSLIQUID204
62106-1125-8Unda 261 in 1 CARTONLIQUID14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62106-1125UNDA 26 (MYRTUS COMMUNIS, APIS MELLIFICA, ARGENTUM METALLICUM) LIQUID [SEROYAL USA]4Current NDC, Legacy NDC, 2 package rows20221110_0fdad876-04c6-13b3-e054-00144ff88e88.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
APIS MELLIFERAACTIVE INGREDIENT7S82P3R43Z1
MYRTUS COMMUNIS TOPACTIVE INGREDIENT367E55FXGW1
SILVERACTIVE INGREDIENT3M4G523W1G1
APIS MELLIFERAACTIVE MOIETY7S82P3R43Z1
MYRTUS COMMUNIS TOPACTIVE MOIETY367E55FXGW1
SILVERACTIVE MOIETY3M4G523W1G1
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62106-112562106-1125-8

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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 26MYRTUS COMMUNIS, APIS MELLIFICA, ARGENTUM METALLICUMSeroyal USA0fdad876-04c6-13b3-e054-00144ff88e882022-11-09WarningsExact identifier
ndc (package): 62106-1125-8
ndc (product): 62106-1125
ndc11 (package): 62106112508
spl id: ed106c48-b013-392c-e053-2995a90ab778
spl set id: 0fdad876-04c6-13b3-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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