PASSIFLORA PLEX- passiflora incarnata, ignatia amara, jalapa, coffea cruda, magnesium metalicum, palladium metallicum, tellurium metallicum, phosphoricum acidum liquid
UNDA

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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PASSIFLORA PLEX

Active ingredients

Each drop contains:

Coffea cruda (Coffee) Seed 10X

Ignatia amara (St. Ignatius’ bean) Seed 8X

Jalapa (Jalap) Tuber 8X

Magnesium metallicum (Magnesium) 10X

Passiflora incarnata (Passion flower) Aerial Parts 3X

Phosphoricum acidum (Phosphoric acid) 14X

Palladium metallicum (Palladium) 10X

Tellurium metallicum (Tellurium) 10X

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Uses

For the temporary relief of symptoms associated with irregular sleep patterns and ordinary restlessness.

Uses

For the temporary relief of symptoms associated with irregular sleep patterns and ordinary restlessness.

Directions

To be taken ten minutes away from food.

Invert bottle and shake lightly allowing drops to fall directly under the tongue or into ¼ oz of water.

Hold contents for about 20 seconds and swallow.

To promote drop flow, invert bottle and shake before each use.

Dosage frequency may be increased up to six times daily depending on the severity of symptoms.

Adults and adolescents (12 years and older) Take 10 drops three times daily or as recommended by your healthcare practitioner.

Children (under 12 years) .Take under the direction of your healthcare practitioner.

Directions

To be taken ten minutes away from food.

Invert bottle and shake lightly allowing drops to fall directly under the tongue or into ¼ oz of water.

Hold contents for about 20 seconds and swallow.

To promote drop flow, invert bottle and shake before each use.

Dosage frequency may be increased up to six times daily depending on the severity of symptoms.

Adults and adolescents (12 years and older) Take 10 drops three times daily or as recommended by your healthcare practitioner.

Children (under 12 years) .Take under the direction of your healthcare practitioner.

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.

Inactive ingredients

Ethanol (beet), purified water

NDC 62106-1322-0

UNDA

PLEX

PASSIFLORA PLEX

Homeopathic Preparation

For the temporary relief of symptoms associated with irregular sleep patterns and ordinary restlessness.

Contains 60% Alcohol

1 fl oz (30 ML)

62106-1322-0

PASSIFLORA PLEX
passiflora incarnata, ignatia amara, jalapa, coffea cruda, magnesium metalicum, palladium metallicum, tellurium metallicum, phosphoricum acidum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:52503-1322
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
PASSIFLORA INCARNATA FLOWERING TOP (UNII: CLF5YFS11O) (PASSIFLORA INCARNATA FLOWERING TOP - UNII:CLF5YFS11O)	PASSIFLORA INCARNATA FLOWERING TOP	3 [hp_X] in 30 mL
ARABICA COFFEE BEAN (UNII: 3SW678MX72) (ARABICA COFFEE BEAN - UNII:3SW678MX72)	ARABICA COFFEE BEAN	10 [hp_X] in 30 mL
MAGNESIUM (UNII: I38ZP9992A) (MAGNESIUM - UNII:I38ZP9992A)	MAGNESIUM	10 [hp_X] in 30 mL
STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (STRYCHNOS IGNATII SEED - UNII:1NM3M2487K)	STRYCHNOS IGNATII SEED	8 [hp_X] in 30 mL
IPOMOEA PURGA ROOT (UNII: 4UDO46YBK2) (IPOMOEA PURGA ROOT - UNII:4UDO46YBK2)	IPOMOEA PURGA ROOT	8 [hp_X] in 30 mL
PALLADIUM (UNII: 5TWQ1V240M) (PALLADIUM - UNII:5TWQ1V240M)	PALLADIUM	10 [hp_X] in 30 mL
TELLURIUM (UNII: NQA0O090ZJ) (TELLURIUM - UNII:NQA0O090ZJ)	TELLURIUM	10 [hp_X] in 30 mL
PHOSPHORIC ACID (UNII: E4GA8884NN) (PHOSPHORIC ACID - UNII:E4GA8884NN)	PHOSPHORIC ACID	14 [hp_X] in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)	12.07 g in 30 mL
ALCOHOL (UNII: 3K9958V90M)	14.94 g in 30 mL

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:52503-1322-0	1 in 1 CARTON	02/09/2015
1		30 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		02/09/2015

Labeler - UNDA (400346069)

Name	Address	ID/FEI	Business Operations
Establishment
UNDA		400346069	manufacture(52503-1322)

Revised: 9/2019

Document Id: 937b6700-3ba9-0266-e053-2995a90a3318

Set id: 937b6700-3ba8-0266-e053-2995a90a3318

Version: 1

Effective Time: 20190926

UNDA