UNDA 1002

Manufacturer
Seroyal USA | SAN’UP
Effective date
2022-11-09
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:18:30

Label at a glance#

ProductUNDA 1002
Active ingredientRANUNCULUS FICARIA, SARSAPARILLA, GARLIC, CYNARA SCOLYMUS LEAF, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, TOXICODENDRON PUBESCENS SHOOT, BRYONIA DIOICA ROOT
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients
Each drop contains:
Allium sativum (Garlic) Bulb 4X
Bryonia dioica Root 6X
Cynara scolymus (Artichoke) Aerial Parts 4X
Hamamelis virginiana (Witch hazel) Bark 4X
Ranunculus ficaria (Lesser celandine) Aerial Parts 4X
Rhus toxicodendron (Poison ivy) Young Shoot 4X
Sarsaparilla Root 4X

OTC - PURPOSE SECTION

Uses
For the temporary relief of symptoms associated with mild joint pain.

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 - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a health professional before use.

OTC - STOP USE SECTION

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

OTHER SAFETY INFORMATION

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

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 mild joint pain.

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

62106-117562106-1175

NDC 62106-1175-8

UNDA

numbered compounds

UNDA 1002

Homeopathic Preparation

For the temporary relief of symptoms
associated with mild joint pain.

Contains 31% Alcohol
0.7 fl oz (20 ml)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62106-1175-8UNDA 100220 mL in 1 BOTTLE, GLASSLIQUID203
62106-1175-8UNDA 10021 in 1 CARTONLIQUID13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62106-1175UNDA 1002 (ALLIUM SATIVUM, BRYONIA DIOICA, CYNARA SCOLYMUS, HAMAMELIS VIRGINIANA, RANUNCULUS FICARIA, RHUS TOXICODENDRON, SARSAPARILLA) LIQUID [SEROYAL USA]3Current NDC, Legacy NDC, 2 package rows20221111_6b64ef65-b970-ff8e-e053-2991aa0a43cb.zip

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
62106-117562106-1175-8

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

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 1002ALLIUM SATIVUM, BRYONIA DIOICA, CYNARA SCOLYMUS, HAMAMELIS VIRGINIANA, RANUNCULUS FICARIA, RHUS TOXICODENDRON, SARSAPARILLASeroyal USA6b64ef65-b970-ff8e-e053-2991aa0a43cb2022-11-09WarningsExact identifier
ndc (package): 62106-1175-8
ndc (product): 62106-1175
ndc11 (package): 62106117508
spl id: ed13065b-c454-641d-e053-2a95a90ace02
spl set id: 6b64ef65-b970-ff8e-e053-2991aa0a43cb

Reported adverse events (FAERS/openFDA)#

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