UNDA 32

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 02:18:28

Label at a glance#

ProductUNDA 32
Active ingredientSILVER, TIN, ACONITUM NAPELLUS, BORAGE, GRINDELIA HIRSUTULA FLOWERING TOP, CAMPHOR (NATURAL)
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients
Each drop contains:
Aconitum napellus (Aconite) Whole Plant 4X
Argentum metallicum (Silver) 12X
Borago officinalis (Common borage) Leaf 4X
Camphora (Camphor from Cinnamomum camphora) 4X
Grindelia Aerial Parts 4X
Stannum metallicum (Tin) 12X

OTC - PURPOSE SECTION

Uses
For the temporary relief of cough.

WARNINGS SECTION

Warnings
Ask a doctor before use if you have
Persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema.
Cough that is accompanied by excessive phlegm (mucus) or fever.

Stop use and ask a doctor if

Cough persists for more than 1 week, tends to recur, or is accompanied by a fever, rash, or persistent headache. A
persistent cough may be a sign of a serious condition.
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 - ASK DOCTOR SECTION

Ask a doctor before use if you have
Persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema.
Cough that is accompanied by excessive phlegm (mucus) or fever.

OTC - STOP USE SECTION

Stop use and ask a doctor if
Cough persists for more than 1 week, tends to recur, or is accompanied by a fever, rash, or persistent headache. A persistent cough may be a sign of a serious condition.

Symptoms persist or worsen.

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. In case of overdose, get medical help or contact a Poison Control Center right away.

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 cough.

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

62106-113162106-1131

NDC 62106-1131-8

UNDA

numbered compounds

UNDA 32

Homeopathic Preparation

For the temporary relief of cough.

Contains 31% Alcohol

0.7 fl oz (20 ml)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62106-1131-8UNDA 321 in 1 CARTONLIQUID13
62106-1131-8UNDA 3220 mL in 1 BOTTLE, GLASSLIQUID203

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62106-1131UNDA 32 (ACONITUM NAPELLUS, ARGENTUM METALLICUM,BORAGO OFFICINALIS, CAMPHORA, GRINDELIA, STANNUM METALLICUM) LIQUID [SEROYAL USA]3Current NDC, Legacy NDC, 2 package rows20221110_3d1dabe8-2b1b-52dd-e054-00144ff88e88.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62106-113162106-1131-8

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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 32ACONITUM NAPELLUS, ARGENTUM METALLICUM,BORAGO OFFICINALIS, CAMPHORA, GRINDELIA, STANNUM METALLICUMSeroyal USA3d1dabe8-2b1b-52dd-e054-00144ff88e882022-11-09WarningsExact identifier
ndc (package): 62106-1131-8
ndc (product): 62106-1131
ndc11 (package): 62106113108
spl id: ed108a25-7e6b-6b6d-e053-2995a90a0e11
spl set id: 3d1dabe8-2b1b-52dd-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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