Unda 42

Manufacturer
Seroyal USA | SAN’UP
Effective date
2021-07-15
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 02:14:42

Label at a glance#

ProductUnda 42
Active ingredientGELSEMIUM SEMPERVIRENS ROOT, ACONITUM NAPELLUS, GOLD, ARNICA MONTANA, COPPER
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients
Each drop contains equal parts of:
Aconitum napellus (Aconite) Whole Plant 4X
Arnica montana (Mountain arnica) Root 4X
Aurum metallicum (Gold) 12X
Cuprum metallicum (Copper) 12X
Gelsemium sempervirens (Yellow jessamine) Root 4X

OTC - PURPOSE SECTION

Uses
For the relief of symptoms
associated with minor back 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 - 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.

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

Indications
For the relief of symptoms associated with minor back 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.

OTHER SAFETY INFORMATION

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

Contents may not fill package in order
to accommodate required labeling.
Please rely on stated quantity.

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Ethanol (beet),
purified water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

62106-1141-862106-1141-8

NDC 62106-1141-8

UNDA

numbered compounds

UNDA 42

Homeopathic Preparation

For the temporary relief of symptoms
associated with minor back pain.

Contains 31% Alcohol

0.7 fl oz (20 mL)

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c599c4a0-705d-4ebb-ab1f-977af038f96aProduct name120251124
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62106-1141-8Unda 421 in 1 CARTONLIQUID16
62106-1141-8Unda 4220 mL in 1 BOTTLE, GLASSLIQUID206

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62106-1141UNDA 42 (ARNICA MONTANA, ACONITUM NAPELLUS, GELSEMIUM SEMPERVIRENS, AURUM METALLICUM, CUPRUM METALLICUM) LIQUID [SEROYAL USA]6Current NDC, Legacy NDC, 2 package rows20210717_0cca91ac-7795-517c-e054-00144ff8d46c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ACONITUM NAPELLUSACTIVE INGREDIENTU0NQ8555JD1
ARNICA MONTANAACTIVE INGREDIENTO80TY208ZW1
COPPERACTIVE INGREDIENT789U1901C51
GELSEMIUM SEMPERVIRENS ROOTACTIVE INGREDIENT639KR60Q1Q1
GOLDACTIVE INGREDIENT79Y1949PYO1
ACONITUM NAPELLUSACTIVE MOIETYU0NQ8555JD1
ARNICA MONTANAACTIVE MOIETYO80TY208ZW1
COPPERACTIVE MOIETY789U1901C51
GELSEMIUM SEMPERVIRENS ROOTACTIVE MOIETY639KR60Q1Q1
GOLDACTIVE MOIETY79Y1949PYO1
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
62106-114162106-1141-8

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 42ARNICA MONTANA, ACONITUM NAPELLUS, GELSEMIUM SEMPERVIRENS, AURUM METALLICUM, CUPRUM METALLICUMSeroyal USA0cca91ac-7795-517c-e054-00144ff8d46c2021-07-15WarningsExact identifier
ndc (package): 62106-1141-8
ndc (product): 62106-1141
ndc11 (package): 62106114108
spl id: c7333ab3-5b52-3805-e053-2995a90a48fc
spl set id: 0cca91ac-7795-517c-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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