OTC - ACTIVE INGREDIENT SECTION
Active ingredients
Each drop contains:
Crataegus (Hawthorn) Fruit 4X
Magnolia grandiflora (Bull bay) Flower 4X
Passiflora incarnata (Passion flower) Aerial Parts 4X
Strophanthus gratus Seed 4X
UNDA 248
- 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 02:18:29
Label at a glance#
ProductUNDA 248
Active ingredientSTROPHANTHUS GRATUS SEED, CRATAEGUS FRUIT, MAGNOLIA GRANDIFLORA FLOWER, PASSIFLORA INCARNATA FLOWERING TOP
Label structure10 sections
Label contents#
Full prescribing information#
OTC - PURPOSE SECTION
Uses
For the temporary relief of overall poor circulation symptoms.
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.
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 overall poor circulation symptoms.
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
NDC 62106-1164-8
UNDA
numbered compounds
UNDA 248
Homeopathic Preparation
For the temporary relief of overall poor circulation symptoms.
Contains 31% Alcohol
0.7 fl oz (20 ml)
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 62106-1164-8 | UNDA 248 | 1 in 1 CARTON | LIQUID | 1 | 3 | |
| 62106-1164-8 | UNDA 248 | 20 mL in 1 BOTTLE, GLASS | LIQUID | 20 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 62106-1164 | UNDA 248 (CRATAEGUS, MAGNOLIA GRANDIFLORA, PASSIFLORA INCARNATA, STROPHANTHUS GRATUS) LIQUID [SEROYAL USA] | 3 | Current NDC, Legacy NDC, 2 package rows | 20221110_5383e4f9-337a-74b5-e054-00144ff88e88.zip |
Products#
Every source-derived product name is available through these pages.
- UNDA 248
- Crataegus, Magnolia grandiflora, Passiflora incarnata, Strophanthus gratus
- STROPHANTHUS GRATUS SEED
- ALCOHOL
- WATER
- CRATAEGUS FRUIT
- MAGNOLIA GRANDIFLORA FLOWER
- PASSIFLORA INCARNATA FLOWERING TOP
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 62106-1164 | 62106-1164-8 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| STROPHANTHUS GRATUS SEED | S81N5ILG2E | ACTIB |
| ALCOHOL | 3K9958V90M | IACT |
| WATER | 059QF0KO0R | IACT |
| CRATAEGUS FRUIT | Q21UUL2105 | ACTIB |
| MAGNOLIA GRANDIFLORA FLOWER | RV23PE6426 | ACTIB |
| PASSIFLORA INCARNATA FLOWERING TOP | CLF5YFS11O | ACTIB |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| UNDA 248 | CRATAEGUS, MAGNOLIA GRANDIFLORA, PASSIFLORA INCARNATA, STROPHANTHUS GRATUS | Seroyal USA | 5383e4f9-337a-74b5-e054-00144ff88e88 | 2022-11-09 | Warnings | 62106-1164-8 62106-1164 62106116408 ed123cdf-4e72-2c64-e053-2995a90a59e3 5383e4f9-337a-74b5-e054-00144ff88e88 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.