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Bio Placenta Phase

Deseret Biologicals, Inc.
Apotheca Company

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENTS:

Aesculus hippocastanum 4X, Sarcolacticum acidum 4X, Secale cornutum 4X, Cuprum sulphuricum 6X, Melilotus officinalis 6X, Placenta totalis suis 6X, Solanum nigrum 6X, Strophanthus hispidus 6X, DHEA (Dehydroepiandrosterone) 12X, 30X, 200X, 12C, 30C, 60C, 200C, Quercetin 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Rutin 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Natrum pyruvicum 8X, Vein (suis) 8X, Artery (suis) 10X, Funiculus umbilicalis suis 10X, Tabacum 10X, Vipera berus 10X, Baryta carbonica 13X, Plumbum iodatum 18X, Astragalus excapus 6C, Proteus (Vulgaris) 30C.

INDICATIONS:

For the temporary relief of symptoms related to chronic poor circulation, low energy, poor wound healing and insomnia.

WARNINGS:

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

If pregnant or breast-feeding, ask a health professional before use.

Tamper seal:  "Sealed for Your Protection."  Do not use if seal is boken or missing.

KEEP OUT OF REACH OF CHILDREN:

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

DIRECTIONS:

1-10 drops under the tongue, 2 times a day or as directed by a health professional.  Consult a physician for use in children under 12 years of age.

INDICATIONS:

For the temporary relief of symptoms related to chronic poor circulation, low energy, poor wound healing and insomnia.

INACTIVE INGREDIENTS:

Demineralized Water, 25% Ethanol

QUESTIONS:

Dist. By: Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070     wwwdesbio.com

PACKAGE LABEL DISPLAY:

DESBIO

NDC 43742-0407-1

HOMEOPATHIC

BIO PLACENTA PHASE

1 FL OZ (30 ml)

Bio Placenta Phase

Bio Placenta Phase

Aesculus hippocastanum, Sarcolacticum acidum, Secale cornutum, Cuprum sulphuricum, Melilotus officinalis, Placenta totalis suis, Solanum nigrum, LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:43742-0407
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
HORSE CHESTNUT HORSE CHESTNUT 4 [hp_X]
LACTIC ACID, L- LACTIC ACID, L- 4 [hp_X]
CLAVICEPS PURPUREA SCLEROTIUM CLAVICEPS PURPUREA SCLEROTIUM 4 [hp_X]
CUPRIC SULFATE CUPRIC CATION 6 [hp_X]
MELILOTUS OFFICINALIS TOP MELILOTUS OFFICINALIS TOP 6 [hp_X]
SUS SCROFA PLACENTA SUS SCROFA PLACENTA 6 [hp_X]
SOLANUM NIGRUM WHOLE SOLANUM NIGRUM WHOLE 6 [hp_X]
STROPHANTHUS HISPIDUS SEED STROPHANTHUS HISPIDUS SEED 6 [hp_X]
PRASTERONE PRASTERONE 12 [hp_X]
QUERCETIN QUERCETIN 12 [hp_X]
RUTIN 6 [hp_X]
Sodium Pyruvate PYRUVIC ACID 8 [hp_X]
SUS SCROFA VEIN SUS SCROFA VEIN 8 [hp_X]
SUS SCROFA ARTERY SUS SCROFA ARTERY 10 [hp_X]
SUS SCROFA UMBILICAL CORD SUS SCROFA UMBILICAL CORD 10 [hp_X]
TOBACCO LEAF TOBACCO LEAF 10 [hp_X]
Vipera Berus Venom Vipera Berus Venom 10 [hp_X]
BARIUM CARBONATE BARIUM CATION 13 [hp_X]
LEAD IODIDE LEAD IODIDE 18 [hp_X]
PROTEUS VULGARIS PROTEUS VULGARIS 30 [hp_C]

Inactive Ingredients

Ingredient Name Strength
water
ALCOHOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:43742-0407-1 30 in 1 BOTTLE, DROPPER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2014-05-22


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