Unda 233

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 02:18:24

Label at a glance#

ProductUnda 233
Active ingredientRHEUM TANGUTICUM WHOLE, HAWTHORN LEAF WITH FLOWER, ARCTOSTAPHYLOS UVA-URSI LEAF, TOXICODENDRON PUBESCENS LEAF, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients
Each drop contains:
Crataegus (Hawthorn) Fruit 4X
Hamamelis virginiana (Witch Hazel) Bark 4X
Rheum (Chinese Rhubarb) Underground Parts 4X.
Rhus toxicodendron (Poison Ivy) Shoots 4X
Uva-ursi (Bearberry) Leaf 4X

OTC - PURPOSE SECTION

Uses
For the temporary relief of symptoms
associated with varicose veins.

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 symptoms
associated with varicose vein problems.

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

62106-1160-862106-1160-8

NDC 62106-1160-8

UNDA

numbered compounds

UNDA 233

Homeopathic Preparation

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
62106-1160-8Unda 2331 in 1 CARTONLIQUID14
62106-1160-8Unda 23320 mL in 1 BOTTLE, GLASSLIQUID204

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62106-1160UNDA 233 (RHEUM, CRATAEGUS, UVA-URSI, RHUS TOXICODENDRON, HAMAMELIS VIRGINIANA) LIQUID [SEROYAL USA]4Current NDC, Legacy NDC, 2 package rows20221110_0ccb5ad0-9604-0018-e054-00144ff8d46c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ARCTOSTAPHYLOS UVA-URSI LEAFACTIVE INGREDIENT3M5V3D1X361
HAMAMELIS VIRGINIANA ROOT BARK/STEM BARKACTIVE INGREDIENTT7S323PKJS1
HAWTHORN LEAF WITH FLOWERACTIVE INGREDIENT6OM09RPY361
RHEUM TANGUTICUM WHOLEACTIVE INGREDIENTQH89N6B02U1
TOXICODENDRON PUBESCENS LEAFACTIVE INGREDIENT6IO182RP7A1
ARCTOSTAPHYLOS UVA-URSI LEAFACTIVE MOIETY3M5V3D1X361
HAMAMELIS VIRGINIANA ROOT BARK/STEM BARKACTIVE MOIETYT7S323PKJS1
HAWTHORN LEAF WITH FLOWERACTIVE MOIETY6OM09RPY361
RHEUM TANGUTICUM WHOLEACTIVE MOIETYQH89N6B02U1
TOXICODENDRON PUBESCENS LEAFACTIVE MOIETY6IO182RP7A1
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62106-116062106-1160-8

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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 233RHEUM, CRATAEGUS, UVA-URSI, RHUS TOXICODENDRON, HAMAMELIS VIRGINIANASeroyal USA0ccb5ad0-9604-0018-e054-00144ff8d46c2022-11-09WarningsExact identifier
ndc (package): 62106-1160-8
ndc (product): 62106-1160
ndc11 (package): 62106116008
spl id: ed11cd4e-d7ca-8446-e053-2995a90afd6e
spl set id: 0ccb5ad0-9604-0018-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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