Unda 47 Liquid
FDA Label NDC 62106-1146

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Seroyal Usa for the product Unda 47 (NDC 62106-1146). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, warnings, otc - stop use, otc - pregnancy or breast feeding, otc - keep out of reach of children, overdosage, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Otc - Active Ingredient

→ Otc - Purpose

→ Warnings

→ Otc - Stop Use

→ Otc - Pregnancy Or Breast Feeding

→ Otc - Keep Out Of Reach Of Children

→ Overdosage

→ Inactive Ingredient

→ Other Safety Information

→ Dosage & Administration

→ Indications & Usage

→ Package Label.principal Display Panel

Otc - Active Ingredient

Active ingredients

Each drop contains:

Absinthium (Common wormwood) Aerial Parts 6X
Arnica montana (Mountain arnica) Underground Parts 6X
Aurum metallicum (Gold) 12X
Jateorhiza palmata (Columbo) Root 6X
Rosmarinus officinalis (Rosemary) Leaf 6X
Stibium metallicum (Antimony) 15X
Thymus vulgaris Aerial Parts 6X
Valeriana officinalis (Valerian) Root 6X

Active ingredients

Each drop contains:

Aluminium metallicum (Aluminum) 12X
Asperula odorata (Sweet woodruff) Aerial Parts 4X
Equisetum arvense (Common horsetail) Stem 4X
Jateorhiza palmata (Columbo) Root 4X
Marrubium vulgare (Common horehound) Aerial Parts 4X
Ocimum basilicum Aerial Parts 4X
Stannum metallicum (Tin) 12X

Otc - Purpose

Uses
For the temporary relief of symptoms associated with dizziness, mental fatigue and nervousness.

Uses

For the temporary relief of symptoms associated with poor digestion.

Warnings

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

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

Otc - Pregnancy Or Breast Feeding

If pregnant or breastfeeding, ask a health professional before use.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Overdosage

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

Inactive Ingredient

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

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

UsesUses
For the temporary relief of symptoms associated with dizziness, mental fatigue and nervousness.

Uses

For the temporary relief of symptoms associated with poor digestion.

Package Label.Principal Display Panel

NDC 62106-1146-8

UNDA

numbered compounds
UNDA 47
Homeopathic Preparation

For the temporary relief of symptoms
associated with dizziness, mental
fatigue and nervousness.
Contains 31% Alcohol
0.7 fl oz (20 ml)

NDC 62106-1142-8

UNDA
numbered compounds
UNDA 43
Homeopathic Preparation

For the temporary relief of symptoms
associated with poor digestion.
Contains 31% Alcohol
0.7 fl oz (20 ml)

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