UNDA 600

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 600

Active ingredientRHEUM OFFICINALE ROOT, BERBERIS VULGARIS ROOT BARK, TOXICODENDRON PUBESCENS SHOOT

Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients
Each drop contains:
Berberis vulgaris (Barberry) Bark 6X
Rheum (Chinese rhubarb) Underground Parts 6X
Rhus toxicodendron (Poison ivy) Young Shoot 6X

OTC - PURPOSE SECTION

Uses
For the temporary relief of occasional muscle stiffness.

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. 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.

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 occasional muscle stiffness.

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

62106-1170-8NDC 62106-1170-8

UNDA

numbered compounds

UNDA

600

Homeopathic Preparation

For the temporary relief of occasional muscle stiffness.

Contains 31% Alcohol

0.7 fl oz (20 ml)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
62106-1170-8	UNDA 600	1 in 1 CARTON	LIQUID	1		3
62106-1170-8	UNDA 600	20 mL in 1 BOTTLE, GLASS	LIQUID	20		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62106-1170	UNDA 600 (BERBERIS VULGARIS, RHEUM, RHUS TOXICODENDRON) LIQUID [SEROYAL USA]	3	Current NDC, Legacy NDC, 2 package rows	20221111_4d505bd6-2819-6c7f-e054-00144ff88e88.zip

Products#

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

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

UNDA 600
Berberis vulgaris, Rheum, Rhus toxicodendron
RHEUM OFFICINALE ROOT
WATER
ALCOHOL
BERBERIS VULGARIS ROOT BARK
TOXICODENDRON PUBESCENS SHOOT

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
62106-1170	62106-1170-8

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
RHEUM OFFICINALE ROOT	A47JP5ZG9M	ACTIB
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	IACT
BERBERIS VULGARIS ROOT BARK	1TH8Q20J0U	ACTIB
TOXICODENDRON PUBESCENS SHOOT	46PYZ1F82M	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
UNDA 600	BERBERIS VULGARIS, RHEUM, RHUS TOXICODENDRON	Seroyal USA	4d505bd6-2819-6c7f-e054-00144ff88e88	2022-11-09	Warnings	Exact identifier ndc (package): 62106-1170-8 ndc (product): 62106-1170 ndc11 (package): 62106117008 spl id: ed12a71d-e8f3-b336-e053-2a95a90a4f09 spl set id: 4d505bd6-2819-6c7f-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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