UNDA 25- argentum metallicum, crataegus, gelsemium sempervirens, hamamelis virginiana, magnolia grandiflora, spiraea ulmaria, stannum metallicum, valeriana officinalis liquid UNDA 27- antimonium crudum, borago officinalis, cetraria islandica, drosera, mentha piperita, senega officinalis liquid UNDA 22- absinthium, aconitum napellus, argentum metallicum, boldo leaf, chamomilla, coffea tosta, jateorhiza palmata, manganum oxydatum nigrum, salvia officinalis liquid UNDA 12- argentum metallicum, aurum metallicum, dulcamara, fagopyrum esculentum, illicium verum, lappa major, salvia officinalis, sarsaparilla, staphysagria, viola tricolor liquid

UNDA 12 by

Drug Labeling and Warnings

UNDA 12 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
Aurum metallicum (Gold) 12X
Dulcamara (Bittersweet) Shoots 4X
Fagopyrum esculentum Aerial Parts 4X
Illicium verum (Star Anise) Fruit 4X
Lappa major (Great burdock) Root 4X
Salvia officinalis (Garden sage) Leaf 4X
Sarsaparilla Root 4X
Staphysagria (Stavesacre) Seed 12X
Viola tricolor (Pansy) Aerial Parts 4X

PURPOSE

Uses

For the temporary relief of symptoms associated with mild skin irritation.

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.

STOP USE

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

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 skin irritation.

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:

Absinthium (Common wormwood) Aerial Parts 4X
Aconitum napellus (Aconite) Whole Plant 4X
Argentum metallicum (Silver) 12X
Boldo Leaf 4X
Chamomilla (German chamomile) Whole Flowering Plant 4X
Coffea tosta (Roasted coffee) Seed 4X
Jateorhiza palmata (Columbo) Root 4X
Manganum oxydatum nigrum (Manganese dioxide) 12X
Salvia officinalis (Garden sage) Leaf 4X

PURPOSE

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

STOP USE

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

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 anxiousness 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.

ACTIVE INGREDIENT

Active ingredients

Each drop contains:
Argentum metallicum (Silver) 12X
Crataegus (Hawthorn) Fruit 4X
Gelsemium sempervirens (Yellow jessamine) Underground Parts 4X
Hamamelis virginiana (Witch hazel) Bark 4X
Magnolia grandiflora Flower 4X
Spiraea ulmaria (Queen-of-the-meadow) Underground Parts 4X
Stannum metallicum (Tin) 12X
Valeriana officinalis (Valerian) Root 4X

PURPOSE

Uses
For the temporary relief of symptoms associated with
coldness or numbness of the extremities.

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.

STOP USE

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
coldness or numbness of the extremities.

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:
Antimonium crudum (Antimonous sulfide) 12X
Borago officinalis (Common borage) Leaf 4X
Cetraria islandica (Iceland moss) Whole Plant 4X
Drosera (Sundew) Whole Plant 4X
Mentha piperita (Peppermint) Aerial Parts 4X
Senega officinalis (Snakeroot) Root 4X

PURPOSE

Uses
For the relief of symptoms associated with laryngitis and voice hoarseness.

WARNINGS

Warnings

Ask a doctor before use if you have Persistent cough or chronic cough
such as occurs with smoking, asthma, chronic bronchitis, or emphysema and Cough that is accompanied by
excessive phlegm (mucus) or fever.

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

STOP USE

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

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

Ask a doctor before use if you have Persistent cough or chronic cough
such as occurs with smoking, asthma, chronic bronchitis, or emphysema and Cough that is accompanied by
excessive phlegm (mucus) or fever.

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 relief of symptoms associated with laryngitis and voice hoarseness.

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: 62106-1152-8

UNDA

numbered compounds

UNDA 12

Homeopathic Preparation

For the temporary relief of symptoms

associated with mild skin irritation.

Contains 31% Alcohol
0.7 fl oz (20 ml)

PRINCIPAL DISPLAY PANEL

NDC: 62106-1121-8

UNDA
numbered compounds
UNDA 22
Homeopathic Preparation

For the temporary relief of symptoms
associated with mild anxiousness
and nervousness.
Contains 31% Alcohol
0.7 fl oz (20 ml)

PRINCIPAL DISPLAY PANEL

NDC: 62106-1124-8

UNDA
numbered compounds
UNDA 25
Homeopathic Preparation

For the temporary relief of symptoms
associated with coldness or numbness
of the extremities.
Contains 31% Alcohol
0.7 fl oz (20 ml)

PRINCIPAL DISPLAY PANEL

UNDA
NDC: 62106-1126-8
numbered compounds
UNDA 27
Homeopathic Preparation

For the relief of symptoms associated with laryngitis and voice hoarseness.
Contains 31% Alcohol
0.7 fl oz (20 mL)

INGREDIENTS AND APPEARANCE

UNDA 25 
argentum metallicum, crataegus, gelsemium sempervirens, hamamelis virginiana, magnolia grandiflora, spiraea ulmaria, stannum metallicum, valeriana officinalis liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62106-1124
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G)	SILVER	12 [hp_X]  in 20 mL
FILIPENDULA ULMARIA ROOT (UNII: 997724QNDS) (FILIPENDULA ULMARIA ROOT - UNII:997724QNDS)	FILIPENDULA ULMARIA ROOT	4 [hp_X]  in 20 mL
CRATAEGUS FRUIT (UNII: Q21UUL2105) (CRATAEGUS FRUIT - UNII:Q21UUL2105)	CRATAEGUS FRUIT	4 [hp_X]  in 20 mL
TIN (UNII: 387GMG9FH5) (TIN - UNII:387GMG9FH5)	TIN	12 [hp_X]  in 20 mL
VALERIAN (UNII: JWF5YAW3QW) (VALERIAN - UNII:JWF5YAW3QW)	VALERIAN	4 [hp_X]  in 20 mL
GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (GELSEMIUM SEMPERVIRENS ROOT - UNII:639KR60Q1Q)	GELSEMIUM SEMPERVIRENS ROOT	4 [hp_X]  in 20 mL
HAMAMELIS VIRGINIANA BARK (UNII: IH3063S9MY) (HAMAMELIS VIRGINIANA BARK - UNII:IH3063S9MY)	HAMAMELIS VIRGINIANA BARK	4 [hp_X]  in 20 mL
MAGNOLIA GRANDIFLORA FLOWER (UNII: RV23PE6426) (MAGNOLIA GRANDIFLORA FLOWER - UNII:RV23PE6426)	MAGNOLIA GRANDIFLORA FLOWER	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: 62106-1124-8	1 in 1 CARTON	09/21/2015
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		09/21/2015

UNDA 27 
antimonium crudum, borago officinalis, cetraria islandica, drosera, mentha piperita, senega officinalis liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62106-1126
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ANTIMONY TRISULFIDE (UNII: F79059A38U) (ANTIMONY TRISULFIDE - UNII:F79059A38U)	ANTIMONY TRISULFIDE	12 [hp_X]  in 20 mL
BORAGE (UNII: PB618V0K2W) (BORAGE - UNII:PB618V0K2W)	BORAGE	4 [hp_X]  in 20 mL
CETRARIA ISLANDICA SUBSP. ISLANDICA (UNII: BJ7YPN79A1) (CETRARIA ISLANDICA SUBSP. ISLANDICA - UNII:BJ7YPN79A1)	CETRARIA ISLANDICA SUBSP. ISLANDICA	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
MENTHA PIPERITA (UNII: 79M2M2UDA9) (MENTHA PIPERITA - UNII:79M2M2UDA9)	MENTHA PIPERITA	4 [hp_X]  in 20 mL
POLYGALA SENEGA ROOT (UNII: M7T6H7D4IF) (POLYGALA SENEGA ROOT - UNII:M7T6H7D4IF)	POLYGALA SENEGA 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: 62106-1126-8	1 in 1 CARTON	09/21/2015
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		09/21/2015

UNDA 22 
absinthium, aconitum napellus, argentum metallicum, boldo leaf, chamomilla, coffea tosta, jateorhiza palmata, manganum oxydatum nigrum, salvia officinalis liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62106-1121
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MANGANESE DIOXIDE (UNII: TF219GU161) (MANGANESE DIOXIDE - UNII:TF219GU161)	MANGANESE DIOXIDE	12 [hp_X]  in 20 mL
SAGE (UNII: 065C5D077J) (SAGE - UNII:065C5D077J)	SAGE	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
MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (MATRICARIA RECUTITA - UNII:G0R4UBI2ZZ)	MATRICARIA RECUTITA	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
WORMWOOD (UNII: F84709P2XV) (WORMWOOD - UNII:F84709P2XV)	WORMWOOD	4 [hp_X]  in 20 mL
ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD)	ACONITUM NAPELLUS	4 [hp_X]  in 20 mL
SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G)	SILVER	12 [hp_X]  in 20 mL
COFFEA ARABICA SEED, ROASTED (UNII: 9H58JRT35E) (COFFEA ARABICA SEED, ROASTED - UNII:9H58JRT35E)	COFFEA ARABICA SEED, ROASTED	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: 62106-1121-8	1 in 1 CARTON	09/21/2015
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		09/21/2015

UNDA 12 
argentum metallicum, aurum metallicum, dulcamara, fagopyrum esculentum, illicium verum, lappa major, salvia officinalis, sarsaparilla, staphysagria, viola tricolor liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62106-1152
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
SOLANUM DULCAMARA TOP (UNII: KPS1B1162N) (SOLANUM DULCAMARA TOP - UNII:KPS1B1162N)	SOLANUM DULCAMARA TOP	4 [hp_X]  in 20 mL
FAGOPYRUM ESCULENTUM (UNII: B10M69172N) (FAGOPYRUM ESCULENTUM - UNII:B10M69172N)	FAGOPYRUM ESCULENTUM	4 [hp_X]  in 20 mL
STAR ANISE FRUIT (UNII: CK15HA8438) (STAR ANISE FRUIT - UNII:CK15HA8438)	STAR ANISE FRUIT	4 [hp_X]  in 20 mL
ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) (ARCTIUM LAPPA ROOT - UNII:597E9BI3Z3)	ARCTIUM LAPPA ROOT	4 [hp_X]  in 20 mL
SAGE (UNII: 065C5D077J) (SAGE - UNII:065C5D077J)	SAGE	4 [hp_X]  in 20 mL
SARSAPARILLA (UNII: 2H1576D5WG) (SARSAPARILLA - UNII:2H1576D5WG)	SARSAPARILLA	4 [hp_X]  in 20 mL
DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV) (DELPHINIUM STAPHISAGRIA SEED - UNII:00543AP1JV)	DELPHINIUM STAPHISAGRIA SEED	12 [hp_X]  in 20 mL
SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G)	SILVER	12 [hp_X]  in 20 mL
VIOLA TRICOLOR (UNII: 9Q24RAI43V) (VIOLA TRICOLOR - UNII:9Q24RAI43V)	VIOLA TRICOLOR	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: 62106-1152-8	1 in 1 CARTON	09/21/2015
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		09/21/2015

Labeler - Seroyal USA (018361118)

Establishment
Name	Address	ID/FEI	Business Operations
SAN’UP		401010287	manufacture(62106-1152, 62106-1121, 62106-1124, 62106-1126)