UNDA 6- senna leaflet, rhamnus frangula bark, carum carvi, foeniculum vulgare, illicium verum, rhamnus cathartica, argentum metallicum liquid UNDA 2- petroselinum sativum, rhamnus frangula, thlaspi bursa-pastoris, juniperus communis, asparagus officinalis, berberis vulgaris, genista tinctoria, argentum metallicum liquid UNDA 295- pulsatilla, nux vomica, aloe socotrina liquid UNDA 9- mentha piperita, melissa officinalis, salvia pratensis, thymus vulgaris, valeriana officinalis, aurum metallicum, plumbum metallicum liquid UNDA 1001- thymus vulgaris, valeriana officinalis, lactuca virosa, passiflora incarnata liquid

UNDA 1001 by

Drug Labeling and Warnings

UNDA 1001 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:
Argentum metallicum (Silver) 12X
Asparagus officinalis (Asparagus) Shoot 4X
Berberis vulgaris (Barberry) Bark 4X
Genista tinctoria Aerial Parts 4X
Juniperus communis (Common juniper) Berry 4X
Petroselinum sativum (Parsley) Whole Plant 4X
Rhamnus frangula (Buckthorn) Bark 4X
Thlaspi bursa-pastoris (Shepherd’s purse) Aerial Parts 4X

PURPOSE

Uses
For the temporary relief of symptoms associated with minor fever.

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.

ASK DOCTOR

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

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

Uses
For the temporary relief of symptoms associated with minor fever.

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:
Argentum metallicum (Silver) 12X
Carum carvi (Caraway) Fruit 4X
Foeniculum vulgare (Fennel) Fruit 4X
Illicium verum (Star anise) Fruit 4X
Rhamnus cathartica (Purging buckthorn) Fruit 4X
Rhamnus frangula (Alder buckthorn) Bark 4X
Senna Leaflet 4X

PURPOSE

Uses

For the temporary relief of symptoms associated with occasional constipation and flatulence.

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 healthcare 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.

ASK DOCTOR

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 occasional constipation and flatulence.

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:
Aurum metallicum (Gold) 12X
Melissa officinalis (Lemon balm) Leaf and Shoot 4X
Mentha piperita Aerial Parts 4X
Plumbum metallicum (Lead) 12X
Salvia pratensis Leaf 4X
Thymus vulgaris Aerial Parts 4X
Valeriana officinalis (Valerian) Root 4X

PURPOSE

Uses
For the temporary relief of symptoms associated with minor stress and mental fatigue.

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.

ASK DOCTOR

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

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

Uses
For the temporary relief of symptoms associated with minor stress and mental fatigue.

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
Nux vomica (Poison nut) Seed 4X
(2.7 x 10-4 % alkaloids, calculated)
Pulsatilla (Wind Flower) Whole Plant 4X

PURPOSE

Uses
For the temporary relief of symptoms associated with mild indigestion.

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.

ASK DOCTOR

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

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

Uses

For the temporary relief of symptoms associated with mild indigestion.

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:
Lactuca virosa
(Poisonous lettuce) Whole Plant 6X
Passiflora incarnata (Passion flower) Aerial Parts 6X
Thymus vulgaris Aerial Parts 6X
Valeriana officinalis (Valerian) Root 6X

PURPOSE

Usea

For the temporary relief of symptoms
associated with mild sleeplessness and nervousness.

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.

ASK DOCTOR

If symptoms persist or worsen, consult your healthcare practitioner.

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

Uses

For the temporary relief of symptoms
associated with mild sleeplessness and nervousness.

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: 62106-1101-8

UNDA

numbered compounds

UNDA 2

Homeopathic Preparation

For the temporary relief of symptoms
associated with minor fever.

Contains 31% Alcohol

0.7 fl oz (20 ml)

PRINCIPAL DISPLAY PANEL

NDC: 62106-1105-8

UNDA

numbered compounds

UNDA 6

Homeopathic Preparation

For the temporary relief of symptomsassociated

with occasional constipation and flatulence.

Contains 31% Alcohol

0.7 fl oz (20 ml)

PRINCIPAL DISPLAY PANEL

NDC: 62106-1108-8

UNDA

numbered compounds

UNDA 9

Homeopathic Preparation

For the temporary relief of symptoms associated

with minor stress and mental fatigue.

Contains 31% Alcohol
0.7 fl oz (20 ml)

PRINCIPAL DISPLAY PANEL

NDC: 62106-1168-8

UNDA

numbered compounds

UNDA 295

Homeopathic Preparation

For the temporary relief of symptoms
associated with mild indigestion.

Contains 31% Alcohol

0.7 fl oz (20 ml)

PRINCIPAL DISPLAY PANEL

NDC: 62106-1174-8

UNDA

numbered compounds

UNDA 1001

Homeopathic Preparation

For the temporary relief of symptoms
associated with mild sleeplessness and
nervousness.

Contains 31% Alcohol
0.7 fl oz (20 ml)

INGREDIENTS AND APPEARANCE

UNDA 6 
senna leaflet, rhamnus frangula bark, carum carvi, foeniculum vulgare, illicium verum, rhamnus cathartica, argentum metallicum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62106-1105
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SENNA LEAF (UNII: AK7JF626KX) (SENNA LEAF - UNII:AK7JF626KX)	SENNA LEAF	4 [hp_X]  in 20 mL
FRANGULA ALNUS BARK (UNII: S2D77IH61R) (FRANGULA ALNUS BARK - UNII:S2D77IH61R)	FRANGULA ALNUS BARK	4 [hp_X]  in 20 mL
CARAWAY SEED (UNII: W2FH8O2BBE) (CARAWAY SEED - UNII:W2FH8O2BBE)	CARAWAY SEED	4 [hp_X]  in 20 mL
FENNEL SEED (UNII: G3QC02NIE6) (FENNEL SEED - UNII:G3QC02NIE6)	FENNEL SEED	4 [hp_X]  in 20 mL
ILLICIUM VERUM WHOLE (UNII: 52JDS841PX) (ILLICIUM VERUM WHOLE - UNII:52JDS841PX)	ILLICIUM VERUM WHOLE	4 [hp_X]  in 20 mL
RHAMNUS CATHARTICA FRUIT (UNII: B4R1EZ1R1D) (RHAMNUS CATHARTICA FRUIT - UNII:B4R1EZ1R1D)	RHAMNUS CATHARTICA FRUIT	4 [hp_X]  in 20 mL
SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G)	SILVER	12 [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: 62106-1105-8	1 in 1 CARTON	05/26/2015
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		05/26/2015

UNDA 2 
petroselinum sativum, rhamnus frangula, thlaspi bursa-pastoris, juniperus communis, asparagus officinalis, berberis vulgaris, genista tinctoria, argentum metallicum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62106-1101
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U)	BERBERIS VULGARIS ROOT BARK	4 [hp_X]  in 20 mL
PETROSELINUM CRISPUM (UNII: 1WZA4Y92EX) (PETROSELINUM CRISPUM - UNII:1WZA4Y92EX)	PETROSELINUM CRISPUM	4 [hp_X]  in 20 mL
ASPARAGUS (UNII: Z1EJP3037Z) (ASPARAGUS - UNII:Z1EJP3037Z)	ASPARAGUS	4 [hp_X]  in 20 mL
FRANGULA ALNUS BARK (UNII: S2D77IH61R) (FRANGULA ALNUS BARK - UNII:S2D77IH61R)	FRANGULA ALNUS BARK	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
SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G)	SILVER	12 [hp_X]  in 20 mL
GENISTA TINCTORIA (UNII: 1F26HNB59H) (GENISTA TINCTORIA - UNII:1F26HNB59H)	GENISTA TINCTORIA	4 [hp_X]  in 20 mL
JUNIPER BERRY (UNII: O84B5194RL) (JUNIPER BERRY - UNII:O84B5194RL)	JUNIPER BERRY	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: 62106-1101-8	1 in 1 CARTON	05/26/2015
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		05/26/2015

UNDA 295 
pulsatilla, nux vomica, aloe socotrina liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62106-1168
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919)	STRYCHNOS NUX-VOMICA SEED	4 [hp_X]  in 20 mL
ALOE (UNII: V5VD430YW9) (ALOE - UNII:V5VD430YW9)	ALOE	6 [hp_X]  in 20 mL
PULSATILLA VULGARIS (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV)	PULSATILLA VULGARIS	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: 62106-1168-8	1 in 1 CARTON	05/27/2015
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		05/27/2015

UNDA 9 
mentha piperita, melissa officinalis, salvia pratensis, thymus vulgaris, valeriana officinalis, aurum metallicum, plumbum metallicum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62106-1108
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
THYMUS VULGARIS WHOLE (UNII: 8L72OKJ7II) (THYMUS VULGARIS WHOLE - UNII:8L72OKJ7II)	THYMUS VULGARIS WHOLE	4 [hp_X]  in 20 mL
VALERIAN (UNII: JWF5YAW3QW) (VALERIAN - UNII:JWF5YAW3QW)	VALERIAN	4 [hp_X]  in 20 mL
LEAD (UNII: 2P299V784P) (LEAD - UNII:2P299V784P)	LEAD	12 [hp_X]  in 20 mL
MENTHA PIPERITA (UNII: 79M2M2UDA9) (MENTHA PIPERITA - UNII:79M2M2UDA9)	MENTHA PIPERITA	4 [hp_X]  in 20 mL
MELISSA OFFICINALIS (UNII: YF70189L0N) (MELISSA OFFICINALIS - UNII:YF70189L0N)	MELISSA OFFICINALIS	4 [hp_X]  in 20 mL
SALVIA PRATENSIS LEAF (UNII: X621621QQV) (SALVIA PRATENSIS LEAF - UNII:X621621QQV)	SALVIA PRATENSIS 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: 62106-1108-8	1 in 1 CARTON	05/27/2015
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		05/27/2015

UNDA 1001 
thymus vulgaris, valeriana officinalis, lactuca virosa, passiflora incarnata liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62106-1174
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
THYMUS VULGARIS WHOLE (UNII: 8L72OKJ7II) (THYMUS VULGARIS WHOLE - UNII:8L72OKJ7II)	THYMUS VULGARIS WHOLE	6 [hp_X]  in 20 mL
VALERIAN (UNII: JWF5YAW3QW) (VALERIAN - UNII:JWF5YAW3QW)	VALERIAN	6 [hp_X]  in 20 mL
PASSIFLORA INCARNATA FLOWERING TOP (UNII: CLF5YFS11O) (PASSIFLORA INCARNATA FLOWERING TOP - UNII:CLF5YFS11O)	PASSIFLORA INCARNATA FLOWERING TOP	6 [hp_X]  in 20 mL
LACTUCA VIROSA (UNII: 6D74QW4H67) (LACTUCA VIROSA - UNII:6D74QW4H67)	LACTUCA VIROSA	6 [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: 62106-1174-8	1 in 1 CARTON	05/27/2015
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		05/27/2015

Labeler - Seroyal USA (018361118)

Establishment
Name	Address	ID/FEI	Business Operations
SAN’UP		401010287	manufacture(62106-1101, 62106-1105, 62106-1108, 62106-1168, 62106-1174)