UNDA 273

Manufacturer
Seroyal USA | SAN’UP
Effective date
2022-11-09
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:18:27

Label at a glance#

ProductUNDA 220
Active ingredientGRINDELIA HIRSUTULA FLOWERING TOP, PILOCARPUS MICROPHYLLUS LEAF, SAGE, DATURA STRAMONIUM, VALERIAN, POLYGALA SENEGA ROOT, ARNICA MONTANA ROOT, EQUISETUM ARVENSE BRANCH, PERSICARIA PUNCTATA, RUBUS FRUTICOSUS LEAF, VERBASCUM DENSIFLORUM FLOWERING TOP
Label structure24 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Each drop contains:

Grindelia Aerial Parts 6X
Pilocarpus Leaf 6X
Salvia officinalis (Garden sage) Leaf 6X
Senega officinalis Root 6X
Stramonium (Thorn apple) Aerial Parts 6X
Valeriana officinalis (Valerian) Root 6X

OTC - PURPOSE SECTION

Uses
For the temporary relief of symptoms associated with 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 - 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.

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

OTHER SAFETY INFORMATION

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

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 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.

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Each drop contains:

Arnica montana (Mountain Arnica) Root 4X
Equisetum arvense (Common Horsetail) Stem 4X
Polygonum hydropiperoides (Mild water pepper) Whole Plant 4X
Rubus fruticosus (Shrubby blackberry) Leaf 4X
Verbascum densiflorum Aerial Parts 4X

OTC - PURPOSE SECTION

Uses

For the temporary relief of symptoms associated with nervousness.

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 - STOP USE SECTION

Stop use and ask a doctor if 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.

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

OTHER SAFETY INFORMATION

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

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 nervousness.

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

62106-1157-862106-1157-8

NDC 62106-1157-8

UNDA
numbered compounds
UNDA 220
Homeopathic Preparation

For the temporary
relief of symptoms
associated with cough.
Contains 31% Alcohol
0.7 fl oz (20 mL)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

62106-1167-862106-1167-8

NDC 62106-1167-8

UNDA
numbered compounds
UNDA 273
Homeopathic Preparation

For the temporary relief of symptoms associated with nervousness.
Contains 31% Alcohol
0.7 fl oz (20 mL)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62106-1157-8UNDA 22020 mL in 1 BOTTLE, GLASSLIQUID205
62106-1157-8UNDA 2201 in 1 CARTONLIQUID15
62106-1167-8UNDA 27320 mL in 1 BOTTLE, GLASSLIQUID205
62106-1167-8UNDA 2731 in 1 CARTONLIQUID15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62106-1157UNDA 220 (GRINDELIA, PILOCARPUS, SALVIA OFFICINALIS, SENEGA OFFICINALIS, STRAMONIUM, VALERIANA OFFICINALIS) LIQUID UNDA 273 (ARNICA MONTANA, EQUISETUM ARVENSE, POLYGONUM HYDROPIPEROIDES, RUBUS FRUTICOSUS, VERBASCUM DENSIFLORUM) LIQUID [SEROYAL USA]5Current NDC, Legacy NDC, 2 package rows20221110_205c3fb7-bee6-4cbf-e054-00144ff88e88.zip
62106-1167UNDA 220 (GRINDELIA, PILOCARPUS, SALVIA OFFICINALIS, SENEGA OFFICINALIS, STRAMONIUM, VALERIANA OFFICINALIS) LIQUID UNDA 273 (ARNICA MONTANA, EQUISETUM ARVENSE, POLYGONUM HYDROPIPEROIDES, RUBUS FRUTICOSUS, VERBASCUM DENSIFLORUM) LIQUID [SEROYAL USA]5Current NDC, Legacy NDC, 2 package rows20221110_205c3fb7-bee6-4cbf-e054-00144ff88e88.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ARNICA MONTANA ROOTACTIVE INGREDIENTMUE8Y113272
DATURA STRAMONIUMACTIVE INGREDIENTG6W4F0V8Z32
EQUISETUM ARVENSE BRANCHACTIVE INGREDIENT1L0VKZ185E2
GRINDELIA HIRSUTULA FLOWERING TOPACTIVE INGREDIENTIDB0NAZ6AI2
PILOCARPUS MICROPHYLLUS LEAFACTIVE INGREDIENTTY68V0X4KL2
POLYGALA SENEGA ROOTACTIVE INGREDIENTM7T6H7D4IF2
POLYGONUM PUNCTATUMACTIVE INGREDIENTD32E7AXD4R2
RUBUS FRUTICOSUS LEAFACTIVE INGREDIENTYQ2S06L8S92
SAGEACTIVE INGREDIENT065C5D077J2
VALERIANACTIVE INGREDIENTJWF5YAW3QW2
VERBASCUM DENSIFLORUM FLOWERING TOPACTIVE INGREDIENT8LR978PU7Y2
ARNICA MONTANA ROOTACTIVE MOIETYMUE8Y113272
DATURA STRAMONIUMACTIVE MOIETYG6W4F0V8Z32
EQUISETUM ARVENSE BRANCHACTIVE MOIETY1L0VKZ185E2
GRINDELIA HIRSUTULA FLOWERING TOPACTIVE MOIETYIDB0NAZ6AI2
PILOCARPUS MICROPHYLLUS LEAFACTIVE MOIETYTY68V0X4KL2
POLYGALA SENEGA ROOTACTIVE MOIETYM7T6H7D4IF2
POLYGONUM PUNCTATUMACTIVE MOIETYD32E7AXD4R2
RUBUS FRUTICOSUS LEAFACTIVE MOIETYYQ2S06L8S92
SAGEACTIVE MOIETY065C5D077J2
VALERIANACTIVE MOIETYJWF5YAW3QW2
VERBASCUM DENSIFLORUM FLOWERING TOPACTIVE MOIETY8LR978PU7Y2
ALCOHOLINACTIVE INGREDIENT3K9958V90M2
WATERINACTIVE INGREDIENT059QF0KO0R2

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62106-115762106-1157-8
62106-116762106-1167-8

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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 · 4 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
4 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 220GRINDELIA, PILOCARPUS, SALVIA OFFICINALIS, SENEGA OFFICINALIS, STRAMONIUM, VALERIANA OFFICINALISSeroyal USA205c3fb7-bee6-4cbf-e054-00144ff88e882022-11-09WarningsExact identifier
ndc (package): 62106-1157-8
ndc (package): 62106-1167-8
ndc (product): 62106-1157
ndc (product): 62106-1167
ndc11 (package): 62106116708
ndc11 (package): 62106115708
spl id: ed10dfda-193f-7f53-e053-2a95a90a72f7
spl set id: 205c3fb7-bee6-4cbf-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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