UNDA 35- aurum metallicum, corallium rubrum exoskeleton, crataegus, grindelia, hamamelis virginiana, mentha piperita, myrtus communis liquid UNDA 710- apis mellifica, calendula officinalis, lycopodium clavatum, dulcamara, aurum metallicum liquid

UNDA 710 by

Drug Labeling and Warnings

UNDA 710 by is a Homeopathic medication manufactured, distributed, or labeled by Seroyal USA, SAN’UP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients

Each drop contains:
Aurum metallicum (Gold) 12X
Corallium rubrum (Red coral) Exoskeleton 12X
Crataegus (Hawthorn) Fruit 4X
Grindelia Aerial Parts 4X
Hamamelis virginiana (Witch hazel) Bark 4X
Mentha piperita Aerial Parts 4X
Myrtus communis (Myrtle) Leafy Twigs 4X

PURPOSE

Uses
For the temporary relief of symptoms associated with cough.

WARNINGS

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.

PREGNANCY OR BREAST FEEDING

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

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

STOP USE

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.

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.
Contents may not fill package in order to accommodate required labeling. Please rely on stated quantity.

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

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.

ACTIVE INGREDIENT

Active ingredients
Each drop contains:
Apis mellifica (Honeybee) Live Bees 4X
Aurum metallicum (Gold) 12X
Calendula officinalis (Marigold) Flowering Tops 4X
Dulcamara (Bittersweet) Shoots 4X
Lycopodium clavatum (Clubmoss) Spore 4X

PURPOSE

Uses
For the temporary relief of symptoms associated with common colds.

WARNINGS

Warning

Sore throat warning: Severe or persistent sore throat or sore throat accompanied

by high fever, headache, nausea and vomiting maybe serious.

Consult physician promptly.

Do not use more than 2 days or administer to children under 3 years of age unless directed by physician.

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.

DO NOT USE

Do not use more than 2 days or administer to children under 3 years of age unless directed by physician.

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

PREGNANCY OR BREAST FEEDING

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

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

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

Uses
For the temporary relief of symptoms associated with common colds.

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.

OTHER SAFETY INFORMATION

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

PRINCIPAL DISPLAY PANEL

NDC: 62106-1134-8

UNDA

numbered compounds

UNDA 35

Homeopathic Preparation

For the temporary relief of symptoms
associated with cough.

Contains 31% Alcohol
0.7 fl oz (20 mL)

PRINCIPAL DISPLAY PANEL

NDC: 62106-1172-8

UNDA

numbered compounds

UNDA 710

Homeopathic Preparation

For the temporary relief of

symptoms associated with
common colds.

Contains 30% Alcohol
0.7 fl oz (20 ml)

INGREDIENTS AND APPEARANCE

UNDA 35 
aurum metallicum, corallium rubrum exoskeleton, crataegus, grindelia, hamamelis virginiana, mentha piperita, myrtus communis liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62106-1134
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO)	GOLD	12 [hp_X]  in 20 mL
CORALLIUM RUBRUM EXOSKELETON (UNII: 2CA71K0DLE) (CORALLIUM RUBRUM EXOSKELETON - UNII:2CA71K0DLE)	CORALLIUM RUBRUM EXOSKELETON	12 [hp_X]  in 20 mL
CRATAEGUS FRUIT (UNII: Q21UUL2105) (CRATAEGUS FRUIT - UNII:Q21UUL2105)	CRATAEGUS FRUIT	4 [hp_X]  in 20 mL
GRINDELIA HIRSUTULA FLOWERING TOP (UNII: IDB0NAZ6AI) (GRINDELIA HIRSUTULA FLOWERING TOP - UNII:IDB0NAZ6AI)	GRINDELIA HIRSUTULA FLOWERING TOP	4 [hp_X]  in 20 mL
HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK - UNII:T7S323PKJS)	HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK	4 [hp_X]  in 20 mL
MENTHA PIPERITA (UNII: 79M2M2UDA9) (MENTHA PIPERITA - UNII:79M2M2UDA9)	MENTHA PIPERITA	4 [hp_X]  in 20 mL
MYRTUS COMMUNIS TOP (UNII: 367E55FXGW) (MYRTUS COMMUNIS TOP - UNII:367E55FXGW)	MYRTUS COMMUNIS TOP	4 [hp_X]  in 20 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62106-1134-8	1 in 1 CARTON	09/10/2015
1		20 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		09/10/2015

UNDA 710 
apis mellifica, calendula officinalis, lycopodium clavatum, dulcamara, aurum metallicum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62106-1172
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479)	LYCOPODIUM CLAVATUM SPORE	4 [hp_X]  in 20 mL
SOLANUM DULCAMARA TOP (UNII: KPS1B1162N) (SOLANUM DULCAMARA TOP - UNII:KPS1B1162N)	SOLANUM DULCAMARA TOP	4 [hp_X]  in 20 mL
GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO)	GOLD	12 [hp_X]  in 20 mL
CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (CALENDULA OFFICINALIS FLOWERING TOP - UNII:18E7415PXQ)	CALENDULA OFFICINALIS FLOWERING TOP	4 [hp_X]  in 20 mL
APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z)	APIS MELLIFERA	4 [hp_X]  in 20 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62106-1172-8	1 in 1 CARTON	09/10/2015
1		20 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		09/10/2015

Labeler - Seroyal USA (018361118)

Establishment
Name	Address	ID/FEI	Business Operations
SAN’UP		401010287	manufacture(62106-1134, 62106-1172)