UNDA 270

Manufacturer
Seroyal USA | SAN’UP
Effective date
2021-07-15
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:14:43

Label at a glance#

ProductUNDA 270
Active ingredientSOLANUM DULCAMARA STEM, CALENDULA OFFICINALIS FLOWERING TOP, EQUISETUM ARVENSE BRANCH, HYPERICUM PERFORATUM
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients
Each drop contains:
Calendula officinalis (Marigold) Aerial Parts 4X
Dulcamara (Bittersweet) Shoots 4X
Equisetum arvense (Common Horsetail) Stem 4X
Hypericum perforatum (St. John’s Wort) Whole Plant 4X

OTC - PURPOSE SECTION

Uses
For the temporary relief of symptoms associated with
minor skin irritation
occasional headache

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.

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

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
minor skin irritation
occasional headache

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

62106-1166-862106-1166-8

NDC 62106-1166-8

UNDA

numbered compounds

UNDA 270

Homeopathic Preparation

For the temporary relief of symptoms associated

with minor skin irritation and occasional headache.

Contains 31% Alcohol

0.7 fl oz (20 ml)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62106-1166-8UNDA 27020 mL in 1 BOTTLE, GLASSLIQUID203
62106-1166-8UNDA 2701 in 1 CARTONLIQUID13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62106-1166UNDA 270 (CALENDULA OFFICINALIS, DULCAMARA, EQUISETUM ARVENSE, HYPERICUM PERFORATUM) LIQUID [SEROYAL USA]3Current NDC, Legacy NDC, 2 package rows20210717_5bb0acb9-be37-7096-e053-2a91aa0adf1c.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62106-116662106-1166-8

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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 270CALENDULA OFFICINALIS, DULCAMARA, EQUISETUM ARVENSE, HYPERICUM PERFORATUMSeroyal USA5bb0acb9-be37-7096-e053-2a91aa0adf1c2021-07-15WarningsExact identifier
ndc (package): 62106-1166-8
ndc (product): 62106-1166
ndc11 (package): 62106116608
spl id: c733a765-4fc8-33c0-e053-2995a90a499e
spl set id: 5bb0acb9-be37-7096-e053-2a91aa0adf1c

Reported adverse events (FAERS/openFDA)#

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