UNDA 8- hamamelis virginiana, millefolium, equisetum arvense, mercurialis perennis, thlaspi bursa-pastoris, cactus grandiflorus, crataegus, cuprum metallicum liquid UNDA 5- tormentilla, tussilago farfara, adiantum capillus-veneris, glycyrrhiza glabra, drosera, grindelia, inula helenium, cuprum metallicum, argentum metallicum liquid UNDA 14- eucalyptus globulus, inula helenium, jateorhiza palmata, camphora, argentum metallicum, aurum metallicum, cuprum metallicum liquid UNDA 212- menyanthes trifoliata, viola tricolor, hydrastis canadensis, aloe socotrina liquid UNDA 226- urtica dioica, berberis vulgaris, boldo, juniperus communis, aloe socotrina, chelidonium majus liquid UNDA 258- berberis vulgaris, bryonia dioica, lycopodium clavatum, mercurialis annua, hydrastis canadensis, boldo, solidago virgaurea liquid

UNDA 258 by

Drug Labeling and Warnings

UNDA 258 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:

Tormentilla (Bloodwort) Rhizome . 4X
Tussilago farfara (Coltsfoot) Whole Plant . 4X
Adiantum capillus-veneris (Maidenhair) Leaf. 4X
Glycyrrhiza glabra (Licorice) Root . 4X
Drosera (Sundew)Whole Plant . 4X
Grindelia Aerial Parts. 4X
Inula helenium (Elecampane) Root . 4X
Cuprum metallicum(Copper) . 12X
Argentum metallicum(Silver). 12X

PURPOSE

Uses

For the temporary relief of symptoms
associated with common colds.

WARNINGS

Warnings

Sore throat warning: Severe or persistent sore throat or sore throat accompanied by high fever, headache,
nausea and vomiting may be serious.
Consult physician promptly. Do not use more than 2 days or administer to children under 3 years of age unless directed by physician.

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.
And 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.

PREGNANCY OR BREAST FEEDING

If you are pregnant or breastfeeding, ask a healthcare practitioner 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.

ACTIVE INGREDIENT

Active ingredients

Each drop contains:
Cactus grandiflorus (Night-blooming cereus) Stem and Flower 4X
Crataegus (Hawthorn) Fruit 4X
Cuprum metallicum (Copper) 12X
Equisetum arvense (Common horsetail) Stem 4X
Hamamelis virginiana (Witch hazel) Bark 4X
Mercurialis perennis (Dog's mercury) Whole Plant 4X
Millefolium (Yarrow) Aerial Parts 4X
Thlaspi bursa-pastoris (Shepherd’s purse) Aerial Parts 4X

PURPOSE

Uses
For the temporary relief of symptoms associated with overall poor circulation.

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.

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.

STOP USE

Stop use and ask a doctor if symptoms persist or worsen

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 overall poor circulation.

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.

ACTIVE INGREDIENT

Active ingredients
Each drop contains:
Argentum metallicum (Silver) 12X
Aurum metallicum (Gold) 12X
Camphora (Camphor from
Cinnamomum camphora) 4X
Cuprum metallicum (Copper) 12X
Eucalyptus globulus (Fever tree) Leaf 4X
Inula helenium (Elecampane) Root 4X
Jateorhiza palmata (Columbo) Root 4X

PURPOSE

Uses
For the temporary relief of symptoms
associated with low energy and common colds

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 you are pregnant or breastfeeding, ask a healthcare practitioner 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.

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.

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 low energy and 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.

ACTIVE INGREDIENT

Active ingredients

Each drop contains:

Menyanthes trifoliata (Buckbean) Whole Plant . 4X
Viola tricolor (Pansy) Whole Plant. 4X
Hydrastis canadensis (Golden seal) Rhizome and Root . 10X
Aloe socotrina (Aloes) Inspissated Juice. 10X

PURPOSE

Indications
For the relief of symptoms associated with anxiousness.

WARNINGS

Warnings
If you are pregnant or breastfeeding, ask a healthcare practitioner before use.
Keep out of reach of children.
In case of overdose, get medical help or contact a Poison Control Center right away.
If symptoms persist or worsen, consult your healthcare practitioner.

PREGNANCY OR BREAST FEEDING

If you are pregnant or breastfeeding, ask a healthcare practitioner 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.

ASK DOCTOR

If symptoms persist or worsen, consult your healthcare practitioner.

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

Indications
For the relief of symptoms associated with anxiousness.

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:
Aloe Inspissated Juice 6X
Berberis vulgaris (Barberry) Bark 6X
Boldo Leaf 6X
Chelidonium majus (Greater celandine) Root and Rhizome 6X
Juniperus communis (Common juniper) Berry 6X
Urtica dioica (Common nettle) Whole Plant 6X

PURPOSE

Uses

For the temporary relief of symptoms associated with poor digestion and lack of appetite.

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.

PREGNANCY OR BREAST FEEDING

If you are pregnant or breastfeeding, ask a healthcare practitioner 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.

STOP USE

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

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 poor digestion and lack of appetite.

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.

ACTIVE INGREDIENT

Active ingredients
Each drop contains:
Berberis vulgaris (Barberry) Bark 4X
Boldo Leaf 4X
Bryonia dioica (Bryony) Root 4X
Hydrastis canadensis (Goldenseal) Rhizome and Root 4X
Lycopodium clavatum (Clubmoss) Spore 4X
Mercurialis annua Aerial Parts 4X
Solidago virgaurea (Goldenrod) Inflorescences 4X

PURPOSE

Uses
For the temporary relief of symptoms associated with
poor digestion
minor urinary discomfort

WARNINGS

Warnings

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

If you are pregnant or breastfeeding, ask a healthcare practitioner 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 you are pregnant or breastfeeding, ask a healthcare practitioner 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
poor digestion
minor urinary discomfort

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.

PRINCIPAL DISPLAY PANEL

NDC: 62106-1165-8

UNDA

numbered compounds

UNDA 258

Homeopathic Preparation

For the temporary relief of symptoms associated with poor digestion and minor urinary discomfort.

Contains 31% Alcohol
0.7 fl oz (20 ml)

PRINCIPAL DISPLAY PANEL

NDC: 62106-1107-8

UNDA

numbered compounds

UNDA 8

Homeopathic Preparation

For the temporary relief of symptoms
associated with overall poor circulation.

Contains 31% Alcohol
0.7 fl oz (20 ml)

PRINCIPAL DISPLAY PANEL

NDC: 62106-1113-8

UNDA

numbered compounds

UNDA 14

Homeopathic Preparation

For the temporary
relief of symptoms
associated with
low energy and
common colds.

Contains 31% Alcohol
0.7 fl oz (20 ml)

PRINCIPAL DISPLAY PANEL

NDC: 62106-1158-8

UNDA

numbered compounds

UNDA 226

Homeopathic Preparation

For the temporary relief of symptoms associated

with poor digestion and lack of appetite.

Contains 31% Alcohol

0.7 fl oz (20 ml)

PRINCIPAL DISPLAY PANEL

UNDA

numbered compounds

NDC: 62106-1104-8

UNDA 5

Homeopathic Preparation

For the temporary relief of symptoms associated with common colds.

Contains 31% Alcohol
0.7 fl oz (20 ml)

PRINCIPAL DISPLAY PANEL

NDC: 62106-1155-8

UNDA

numbered compounds

UNDA 212

Homeopathic Preparation

For the temporary relief of symptoms associated with anxiousness.

Contains 31% Alcohol

0.7 fl oz (20 mL)

INGREDIENTS AND APPEARANCE

UNDA 8 
hamamelis virginiana, millefolium, equisetum arvense, mercurialis perennis, thlaspi bursa-pastoris, cactus grandiflorus, crataegus, cuprum metallicum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62106-1107
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HAMAMELIS VIRGINIANA BARK (UNII: IH3063S9MY) (HAMAMELIS VIRGINIANA BARK - UNII:IH3063S9MY)	HAMAMELIS VIRGINIANA BARK	4 [hp_X]  in 20 mL
MERCURIALIS PERENNIS (UNII: Q35465A1MA) (MERCURIALIS PERENNIS - UNII:Q35465A1MA)	MERCURIALIS PERENNIS	4 [hp_X]  in 20 mL
CRATAEGUS FRUIT (UNII: Q21UUL2105) (CRATAEGUS FRUIT - UNII:Q21UUL2105)	CRATAEGUS FRUIT	4 [hp_X]  in 20 mL
COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5)	COPPER	12 [hp_X]  in 20 mL
ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK) (ACHILLEA MILLEFOLIUM - UNII:2FXJ6SW4PK)	ACHILLEA MILLEFOLIUM	4 [hp_X]  in 20 mL
EQUISETUM ARVENSE BRANCH (UNII: 1L0VKZ185E) (EQUISETUM ARVENSE BRANCH - UNII:1L0VKZ185E)	EQUISETUM ARVENSE BRANCH	4 [hp_X]  in 20 mL
CAPSELLA BURSA-PASTORIS (UNII: W0X9457M59) (CAPSELLA BURSA-PASTORIS - UNII:W0X9457M59)	CAPSELLA BURSA-PASTORIS	4 [hp_X]  in 20 mL
SELENICEREUS GRANDIFLORUS STEM (UNII: 7114SV0MYK) (SELENICEREUS GRANDIFLORUS STEM - UNII:7114SV0MYK)	SELENICEREUS GRANDIFLORUS STEM	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: 62106-1107-8	1 in 1 CARTON	06/02/2015
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		06/02/2015

UNDA 5 
tormentilla, tussilago farfara, adiantum capillus-veneris, glycyrrhiza glabra, drosera, grindelia, inula helenium, cuprum metallicum, argentum metallicum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62106-1104
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POTENTILLA ERECTA ROOT (UNII: BI896CKT6B) (POTENTILLA ERECTA ROOT - UNII:BI896CKT6B)	POTENTILLA ERECTA ROOT	4 [hp_X]  in 20 mL
ADIANTUM CAPILLUS-VENERIS LEAF (UNII: 4817H7M565) (ADIANTUM CAPILLUS-VENERIS LEAF - UNII:4817H7M565)	ADIANTUM CAPILLUS-VENERIS LEAF	4 [hp_X]  in 20 mL
DROSERA ROTUNDIFOLIA FLOWERING TOP (UNII: 75O014T1HG) (DROSERA ROTUNDIFOLIA FLOWERING TOP - UNII:75O014T1HG)	DROSERA ROTUNDIFOLIA FLOWERING TOP	4 [hp_X]  in 20 mL
GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) (GLYCYRRHIZA GLABRA - UNII:2788Z9758H)	GLYCYRRHIZA GLABRA	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
INULA HELENIUM ROOT (UNII: E55SMD6DA8) (INULA HELENIUM ROOT - UNII:E55SMD6DA8)	INULA HELENIUM ROOT	4 [hp_X]  in 20 mL
COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5)	COPPER	12 [hp_X]  in 20 mL
SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G)	SILVER	12 [hp_X]  in 20 mL
TUSSILAGO FARFARA WHOLE (UNII: 6177A89GA2) (TUSSILAGO FARFARA WHOLE - UNII:6177A89GA2)	TUSSILAGO FARFARA WHOLE	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: 62106-1104-8	1 in 1 CARTON	06/02/2015
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		06/02/2015

UNDA 14 
eucalyptus globulus, inula helenium, jateorhiza palmata, camphora, argentum metallicum, aurum metallicum, cuprum metallicum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62106-1113
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
INULA HELENIUM ROOT (UNII: E55SMD6DA8) (INULA HELENIUM ROOT - UNII:E55SMD6DA8)	INULA HELENIUM ROOT	4 [hp_X]  in 20 mL
JATEORHIZA CALUMBA ROOT (UNII: V36I2B8LD5) (JATEORHIZA CALUMBA ROOT - UNII:V36I2B8LD5)	JATEORHIZA CALUMBA ROOT	4 [hp_X]  in 20 mL
CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941)	CAMPHOR (NATURAL)	4 [hp_X]  in 20 mL
SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G)	SILVER	12 [hp_X]  in 20 mL
GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO)	GOLD	12 [hp_X]  in 20 mL
COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5)	COPPER	12 [hp_X]  in 20 mL
EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (EUCALYPTUS GLOBULUS LEAF - UNII:S546YLW6E6)	EUCALYPTUS GLOBULUS LEAF	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: 62106-1113-8	1 in 1 CARTON	06/02/2015
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		06/02/2015

UNDA 212 
menyanthes trifoliata, viola tricolor, hydrastis canadensis, aloe socotrina liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62106-1155
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENYANTHES TRIFOLIATA (UNII: 7H0QTZ446K) (MENYANTHES TRIFOLIATA - UNII:7H0QTZ446K)	MENYANTHES TRIFOLIATA	4 [hp_X]  in 20 mL
VIOLA TRICOLOR (UNII: 9Q24RAI43V) (VIOLA TRICOLOR - UNII:9Q24RAI43V)	VIOLA TRICOLOR	4 [hp_X]  in 20 mL
GOLDENSEAL (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV)	GOLDENSEAL	10 [hp_X]  in 20 mL
ALOE (UNII: V5VD430YW9) (ALOE - UNII:V5VD430YW9)	ALOE	10 [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: 62106-1155-8	1 in 1 CARTON	06/02/2015
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		06/02/2015

UNDA 226 
urtica dioica, berberis vulgaris, boldo, juniperus communis, aloe socotrina, chelidonium majus liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62106-1158
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PEUMUS BOLDUS LEAF (UNII: Q4EWM09M3O) (PEUMUS BOLDUS LEAF - UNII:Q4EWM09M3O)	PEUMUS BOLDUS LEAF	6 [hp_X]  in 20 mL
URTICA DIOICA (UNII: 710FLW4U46) (URTICA DIOICA - UNII:710FLW4U46)	URTICA DIOICA	6 [hp_X]  in 20 mL
BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U)	BERBERIS VULGARIS ROOT BARK	6 [hp_X]  in 20 mL
JUNIPER BERRY (UNII: O84B5194RL) (JUNIPER BERRY - UNII:O84B5194RL)	JUNIPER BERRY	6 [hp_X]  in 20 mL
ALOE (UNII: V5VD430YW9) (ALOE - UNII:V5VD430YW9)	ALOE	6 [hp_X]  in 20 mL
CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (CHELIDONIUM MAJUS - UNII:7E889U5RNN)	CHELIDONIUM MAJUS	6 [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: 62106-1158-8	1 in 1 CARTON	06/02/2015
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		06/02/2015

UNDA 258 
berberis vulgaris, bryonia dioica, lycopodium clavatum, mercurialis annua, hydrastis canadensis, boldo, solidago virgaurea liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62106-1165
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
MERCURIALIS ANNUA FLOWERING TOP (UNII: 7D28M9SL9B) (MERCURIALIS ANNUA FLOWERING TOP - UNII:7D28M9SL9B)	MERCURIALIS ANNUA FLOWERING TOP	4 [hp_X]  in 20 mL
GOLDENSEAL (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV)	GOLDENSEAL	4 [hp_X]  in 20 mL
PEUMUS BOLDUS LEAF (UNII: Q4EWM09M3O) (PEUMUS BOLDUS LEAF - UNII:Q4EWM09M3O)	PEUMUS BOLDUS LEAF	4 [hp_X]  in 20 mL
SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (SOLIDAGO VIRGAUREA FLOWERING TOP - UNII:5405K23S50)	SOLIDAGO VIRGAUREA FLOWERING TOP	4 [hp_X]  in 20 mL
BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U)	BERBERIS VULGARIS ROOT BARK	4 [hp_X]  in 20 mL
BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B)	BRYONIA ALBA ROOT	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: 62106-1165-8	1 in 1 CARTON	06/02/2015
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		06/02/2015

Labeler - Seroyal USA (018361118)

Establishment
Name	Address	ID/FEI	Business Operations
SAN’UP		401010287	manufacture(62106-1104, 62106-1107, 62106-1113, 62106-1155, 62106-1158, 62106-1165)