Unda 39

Manufacturer
Seroyal USA | SAN’UP
Effective date
2022-10-25
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 02:18:19

Label at a glance#

ProductUnda 39
Active ingredientDRYOPTERIS FILIX-MAS ROOT, ARTEMISIA CINA PRE-FLOWERING TOP, SILVER, ASAFETIDA, WORMWOOD, ONION, TANACETUM VULGARE TOP
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients
Each drop contains:
Absinthium (Common wormwood) Aerial Parts 4X
Allium cepa (Onion) Bulb 4X
Argentum metallicum (Silver) 12X
Asafoetida Gum Resin 4X
Cina Flower-heads 6X
Dryopteris filix-mas Rhizome 6X
Tanacetum vulgare Flower and Leaf 4X

OTC - PURPOSE SECTION

Uses

For the temporary relief of minor symptoms associated with
irritability and anxiousness.

WARNINGS SECTION

Warnings
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.

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 minor symptoms
associated with irritability and anxiousness.

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

Unda 39Unda 39

NDC 62106-1138-8

UNDA

numbered compounds

UNDA 39

Homeopathic Preparation

For the temporary relief of minor
symptoms associated with
irritability and anxiousness.

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
62106-1138-8Unda 3920 mL in 1 BOTTLE, GLASSLIQUID206
62106-1138-8Unda 391 in 1 CARTONLIQUID16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62106-1138UNDA 39 (ASAFOETIDA GUM RESIN,ABSINTHIUM, ALLIUM CEPA, TANACETUM VULGARE AERIAL PARTS, CINA FLOWER-HEADS, DRYOPTERIS FILIX-MAS RHIZOME, ARGENTUM METALLICUM) LIQUID [SEROYAL USA]6Current NDC, Legacy NDC, 2 package rows20221027_0cc8aa90-b341-1f90-e054-00144ff88e88.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ARTEMISIA CINA PRE-FLOWERING TOPACTIVE INGREDIENT28M1820ACT1
ASAFETIDAACTIVE INGREDIENTW9FZA51AS11
DRYOPTERIS FILIX-MAS ROOTACTIVE INGREDIENTC0ZK0RRF5X1
ONIONACTIVE INGREDIENT492225Q21H1
SILVERACTIVE INGREDIENT3M4G523W1G1
TANACETUM VULGARE TOPACTIVE INGREDIENTD52957JQ8M1
WORMWOODACTIVE INGREDIENTF84709P2XV1
ARTEMISIA CINA PRE-FLOWERING TOPACTIVE MOIETY28M1820ACT1
ASAFETIDAACTIVE MOIETYW9FZA51AS11
DRYOPTERIS FILIX-MAS ROOTACTIVE MOIETYC0ZK0RRF5X1
ONIONACTIVE MOIETY492225Q21H1
SILVERACTIVE MOIETY3M4G523W1G1
TANACETUM VULGARE TOPACTIVE MOIETYD52957JQ8M1
WORMWOODACTIVE MOIETYF84709P2XV1
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
WATERINACTIVE INGREDIENT059QF0KO0R1

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
62106-113862106-1138-8

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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 39ASAFOETIDA GUM RESIN,ABSINTHIUM, ALLIUM CEPA, TANACETUM VULGARE AERIAL PARTS, CINA FLOWER-HEADS, DRYOPTERIS FILIX-MAS RHIZOME, ARGENTUM METALLICUMSeroyal USA0cc8aa90-b341-1f90-e054-00144ff88e882022-10-25WarningsExact identifier
ndc (package): 62106-1138-8
ndc (product): 62106-1138
ndc11 (package): 62106113808
spl id: ebe17695-25c1-19f2-e053-2a95a90a66ba
spl set id: 0cc8aa90-b341-1f90-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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