UNDA 700- berberis vulgaris, calcarea fluorica liquid UNDA 312- angelica archangelica, drosera, grindelia, lamium album, pinus sylvestris, rubus fruticosus, senega officinalis liquid

UNDA 312 by

Drug Labeling and Warnings

UNDA 312 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:

Angelica archangelica (European angelica) Root 6X
Drosera (Sundew) Whole Plant 6X
Grindelia (Gum-plant) Aerial Parts 6X
Lamium album (Dead nettle) Aerial Parts 6X
Pinus sylvestris (Scotch pine) Shoots 6X
Rubus fruticosus (Shrubby blackberry) Leaf 6X
Senega officinalis (Snakeroot) Root 6X

PURPOSE

Uses
For the relief of symptoms associated with sore throat.

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.

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.

ASK DOCTOR

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

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.

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

DO NOT USE

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

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 relief of symptoms associated with sore throat.

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 equal parts of:

Berberis vulgaris (Barberry) Bark 4X
Calcarea fluorica (Calcium fluoride) 12X

PURPOSE

Uses
For the relief of symptoms associated with low energy and 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.

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 relief of symptoms associated with low energy and 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.

PRINCIPAL DISPLAY PANEL

UNDA
NDC: 62106-1169-8
numbered compounds
UNDA 312
Homeopathic Preparation

For the relief of symptoms associated with sore throat.
Contains 31% Alcohol
0.7 fl oz (20 mL)

PRINCIPAL DISPLAY PANEL

UNDA
NDC: 62106-1171-8
numbered compounds
UNDA 700
Homeopathic Preparation
Contains 31% Alcohol
0.7 fl oz (20 mL)

INGREDIENTS AND APPEARANCE

UNDA 700 
berberis vulgaris, calcarea fluorica liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62106-1171
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
CALCIUM FLUORIDE (UNII: O3B55K4YKI) (FLUORIDE ION - UNII:Q80VPU408O)	CALCIUM FLUORIDE	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: 62106-1171-8	1 in 1 CARTON	09/23/2015
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		09/23/2015

UNDA 312 
angelica archangelica, drosera, grindelia, lamium album, pinus sylvestris, rubus fruticosus, senega officinalis liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62106-1169
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DROSERA ROTUNDIFOLIA FLOWERING TOP (UNII: 75O014T1HG) (DROSERA ROTUNDIFOLIA FLOWERING TOP - UNII:75O014T1HG)	DROSERA ROTUNDIFOLIA FLOWERING TOP	6 [hp_X]  in 20 mL
GRINDELIA HIRSUTULA FLOWERING TOP (UNII: IDB0NAZ6AI) (GRINDELIA HIRSUTULA FLOWERING TOP - UNII:IDB0NAZ6AI)	GRINDELIA HIRSUTULA FLOWERING TOP	6 [hp_X]  in 20 mL
PINUS SYLVESTRIS LEAFY TWIG (UNII: Q1RGP4UB73) (PINUS SYLVESTRIS LEAFY TWIG - UNII:Q1RGP4UB73)	PINUS SYLVESTRIS LEAFY TWIG	6 [hp_X]  in 20 mL
ANGELICA ARCHANGELICA ROOT (UNII: DTN01M69SN) (ANGELICA ARCHANGELICA ROOT - UNII:DTN01M69SN)	ANGELICA ARCHANGELICA ROOT	6 [hp_X]  in 20 mL
LAMIUM ALBUM (UNII: 046Y1357I6) (LAMIUM ALBUM - UNII:046Y1357I6)	LAMIUM ALBUM	6 [hp_X]  in 20 mL
RUBUS FRUTICOSUS LEAF (UNII: YQ2S06L8S9) (RUBUS FRUTICOSUS LEAF - UNII:YQ2S06L8S9)	RUBUS FRUTICOSUS LEAF	6 [hp_X]  in 20 mL
POLYGALA SENEGA ROOT (UNII: M7T6H7D4IF) (POLYGALA SENEGA ROOT - UNII:M7T6H7D4IF)	POLYGALA SENEGA ROOT	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: 62106-1169-8	1 in 1 CARTON	09/23/2015
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		09/23/2015

Labeler - Seroyal USA (018361118)

Establishment
Name	Address	ID/FEI	Business Operations
SAN’UP		401010287	manufacture(62106-1171, 62106-1169)