Unda 17

Manufacturer
Seroyal USA | SAN’UP
Effective date
2022-11-08
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:18:25

Label at a glance#

ProductUnda 17
Active ingredientJATEORHIZA CALUMBA ROOT, PEUMUS BOLDUS LEAF, FRANGULA ALNUS BARK, VALERIAN, CHAMAELIRIUM LUTEUM ROOT, SOLANUM DULCAMARA STEM, RUMEX CRISPUS ROOT, SILVER
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients
Each drop contains:
Argentum metallicum (Silver) 12X
Boldo Leaf 4X
Dulcamara (Bittersweet) Shoots 4X
Jateorhiza palmata (Columbo) Root 4X
Rhamnus frangula (Buckthorn) Bark 4X
Rumex crispus (Curly dock) Underground Parts 4X
Scabiosa succisa (Devil's Bit) Underground Parts 4X
Valeriana officinalis (Valerian) Root 4X

OTC - PURPOSE SECTION

Uses
For the temporary relief of symptoms associated with
mild skin irritation

poor digestion

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.

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 symptom sassociated with
mild skin irritation

poor digestion

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

62106-1116-862106-1116-8

NDC 62106-1116-8

UNDA

numbered compounds

UNDA 17

Homeopathic Preparation

For the temporary relief of symptoms

associated with mild skin irritation

and poor digestion.

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
62106-1116-8Unda 171 in 1 CARTONLIQUID14
62106-1116-8Unda 1720 mL in 1 BOTTLE, GLASSLIQUID204

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62106-1116UNDA 17 (JATEORHIZA PALMATA, BOLDO LEAF, RHAMNUS FRANGULA, SCABIOSA SUCCISA UNDERGROUND PARTS, VALERIANA OFFICINALIS, DULCAMARA, RUMEX CRISPUS, ARGENTUM METALLICUM) LIQUID [SEROYAL USA]4Current NDC, Legacy NDC, 2 package rows20221110_0e6f9040-2bd2-3fd3-e054-00144ff88e88.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CHAMAELIRIUM LUTEUM ROOTACTIVE INGREDIENTDQV54Y5H3U1
FRANGULA ALNUS BARKACTIVE INGREDIENTS2D77IH61R1
JATEORHIZA CALUMBA ROOTACTIVE INGREDIENTV36I2B8LD51
PEUMUS BOLDUS LEAFACTIVE INGREDIENTQ4EWM09M3O1
RUMEX CRISPUS ROOTACTIVE INGREDIENT9N1RM2S62C1
SILVERACTIVE INGREDIENT3M4G523W1G1
SOLANUM DULCAMARA STEMACTIVE INGREDIENTIR986LE7DF1
VALERIANACTIVE INGREDIENTJWF5YAW3QW1
CHAMAELIRIUM LUTEUM ROOTACTIVE MOIETYDQV54Y5H3U1
FRANGULA ALNUS BARKACTIVE MOIETYS2D77IH61R1
JATEORHIZA CALUMBA ROOTACTIVE MOIETYV36I2B8LD51
PEUMUS BOLDUS LEAFACTIVE MOIETYQ4EWM09M3O1
RUMEX CRISPUS ROOTACTIVE MOIETY9N1RM2S62C1
SILVERACTIVE MOIETY3M4G523W1G1
SOLANUM DULCAMARA STEMACTIVE MOIETYIR986LE7DF1
VALERIANACTIVE MOIETYJWF5YAW3QW1
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
62106-111662106-1116-8

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 17JATEORHIZA PALMATA, BOLDO LEAF, RHAMNUS FRANGULA, SCABIOSA SUCCISA UNDERGROUND PARTS, VALERIANA OFFICINALIS, DULCAMARA, RUMEX CRISPUS, ARGENTUM METALLICUMSeroyal USA0e6f9040-2bd2-3fd3-e054-00144ff88e882022-11-08WarningsExact identifier
ndc (package): 62106-1116-8
ndc (product): 62106-1116
ndc11 (package): 62106111608
spl id: ecfce43b-7241-2f77-e053-2a95a90a26bd
spl set id: 0e6f9040-2bd2-3fd3-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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