UNDA 1000

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 02:18:30

Label at a glance#

ProductUNDA 1000
Active ingredientRUBUS FRUTICOSUS LEAF, CALENDULA OFFICINALIS FLOWERING TOP, DROSERA ROTUNDIFOLIA FLOWERING TOP, SPONGIA OFFICINALIS SKELETON, ROASTED
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients
Calendula officinalis (Marigold) Flowering Tops 4X
Drosera (Sundew) Whole Plant 4X
Rubus fruticosus Leaf 4X
Spongia tosta (Roasted sponge) 4X

OTC - PURPOSE SECTION

Uses

For the temporary relief of minor digestive upset and tiredness.

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.

OTC - STOP USE SECTION

Stop use and ask a doctor if symptoms persist or worsen.

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 minor digestive upset and tiredness.

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

62106-117362106-1173

NDC 62106-1173-8

UNDA
numbered compounds
UNDA 1000
Homeopathic Preparation

For the temporary relief of minor

digestive upset and tiredness.
Contains 31% Alcohol
0.7 fl oz (20 ml)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62106-1173-8UNDA 100020 mL in 1 BOTTLE, GLASSLIQUID204
62106-1173-8UNDA 10001 in 1 CARTONLIQUID14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62106-1173UNDA 1000 (RUBUS FRUTICOSUS, SPONGIA TOSTA, CALENDULA OFFICINALIS, DROSERA) LIQUID [SEROYAL USA]4Current NDC, Legacy NDC, 2 package rows20221111_206b66f0-67e1-5626-e054-00144ff88e88.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CALENDULA OFFICINALIS FLOWERING TOPACTIVE INGREDIENT18E7415PXQ1
DROSERA ROTUNDIFOLIA FLOWERING TOPACTIVE INGREDIENT75O014T1HG1
RUBUS FRUTICOSUS LEAFACTIVE INGREDIENTYQ2S06L8S91
SPONGIA OFFICINALIS SKELETON, ROASTEDACTIVE INGREDIENT1PIP394IID1
CALENDULA OFFICINALIS FLOWERING TOPACTIVE MOIETY18E7415PXQ1
DROSERA ROTUNDIFOLIA FLOWERING TOPACTIVE MOIETY75O014T1HG1
RUBUS FRUTICOSUS LEAFACTIVE MOIETYYQ2S06L8S91
SPONGIA OFFICINALIS SKELETON, ROASTEDACTIVE MOIETY1PIP394IID1
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
WATERINACTIVE INGREDIENT059QF0KO0R1

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
62106-117362106-1173-8

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

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 1000RUBUS FRUTICOSUS, SPONGIA TOSTA, CALENDULA OFFICINALIS, DROSERASeroyal USA206b66f0-67e1-5626-e054-00144ff88e882022-11-09WarningsExact identifier
ndc (package): 62106-1173-8
ndc (product): 62106-1173
ndc11 (package): 62106117308
spl id: ed12fac1-c818-2486-e053-2995a90a0824
spl set id: 206b66f0-67e1-5626-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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