FDA.reportPublic FDA data

Bio Placenta Phase

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2016-10-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 01:22:24

Label at a glance#

ProductBio Placenta Phase
Active ingredientHORSE CHESTNUT, LACTIC ACID, L-, CLAVICEPS PURPUREA SCLEROTIUM, CUPRIC SULFATE, MELILOTUS OFFICINALIS TOP, SUS SCROFA PLACENTA, SOLANUM NIGRUM WHOLE, STROPHANTHUS HISPIDUS SEED, PRASTERONE, QUERCETIN, RUTIN, SODIUM PYRUVATE, SUS SCROFA VEIN, SUS SCROFA ARTERY, SUS SCROFA UMBILICAL CORD, TOBACCO LEAF, VIPERA BERUS VENOM, BARIUM CARBONATE, LEAD IODIDE, ASTRAGALUS EXSCAPUS WHOLE FLOWERING/FRUITING, PROTEUS VULGARIS
Label structure9 sections

Dosage and administration

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.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

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:

OTC - PURPOSE SECTION

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

WARNINGS:

WARNINGS SECTION

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 broken or missing.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

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:

INDICATIONS & USAGE SECTION

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

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, 25% Ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. By: Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070     www.desbio.com

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DESBIO

NDC 43742-0407-1

HOMEOPATHIC

BIO PLACENTA
PHASE

1 FL OZ (30 ml)

Bio Placenta PhaseBio Placenta Phase

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ASTRAGALUS EXSCAPUS WHOLE FLOWERING/FRUITINGACTIVE INGREDIENT0II1G590JE2
BARIUM CARBONATEACTIVE INGREDIENT6P669D8HQ82
CLAVICEPS PURPUREA SCLEROTIUMACTIVE INGREDIENT01G9XEA93N2
CUPRIC SULFATEACTIVE INGREDIENTLRX7AJ16DT2
HORSE CHESTNUTACTIVE INGREDIENT3C18L6RJAZ2
LACTIC ACID, L-ACTIVE INGREDIENTF9S9FFU82N2
LEAD IODIDEACTIVE INGREDIENTOTL90F2GLT2
MELILOTUS OFFICINALIS TOPACTIVE INGREDIENTGM6P02J2DX2
PRASTERONEACTIVE INGREDIENT459AG36T1B2
PROTEUS VULGARISACTIVE INGREDIENT11T9HCO30O2
QUERCETINACTIVE INGREDIENT9IKM0I5T1E2
RUTINACTIVE INGREDIENT5G06TVY3R72
SODIUM PYRUVATEACTIVE INGREDIENTPOD38AIF082
SOLANUM NIGRUM WHOLEACTIVE INGREDIENT0FMD6WV47M2
STROPHANTHUS HISPIDUS SEEDACTIVE INGREDIENTMO892VI77K2
SUS SCROFA ARTERYACTIVE INGREDIENT63O327782Q2
SUS SCROFA PLACENTAACTIVE INGREDIENTC8CV8867O82
SUS SCROFA UMBILICAL CORDACTIVE INGREDIENT118OYG6W3H2
SUS SCROFA VEINACTIVE INGREDIENT2510RH3I892
TOBACCO LEAFACTIVE INGREDIENT6YR2608RSU2
VIPERA BERUS VENOMACTIVE INGREDIENT0ORO6NCA4M2
ASTRAGALUS EXSCAPUS WHOLE FLOWERING/FRUITINGACTIVE MOIETY0II1G590JE2
BARIUM CATIONACTIVE MOIETYV645272HLN2
CLAVICEPS PURPUREA SCLEROTIUMACTIVE MOIETY01G9XEA93N2
CUPRIC CATIONACTIVE MOIETY8CBV67279L2
HORSE CHESTNUTACTIVE MOIETY3C18L6RJAZ2
LACTIC ACID, L-ACTIVE MOIETYF9S9FFU82N2
LEAD IODIDEACTIVE MOIETYOTL90F2GLT2
MELILOTUS OFFICINALIS TOPACTIVE MOIETYGM6P02J2DX2
PRASTERONEACTIVE MOIETY459AG36T1B2
PROTEUS VULGARISACTIVE MOIETY11T9HCO30O2
PYRUVIC ACIDACTIVE MOIETY8558G7RUTR2
QUERCETINACTIVE MOIETY9IKM0I5T1E2
RUTINACTIVE MOIETY5G06TVY3R72
SOLANUM NIGRUM WHOLEACTIVE MOIETY0FMD6WV47M2
STROPHANTHUS HISPIDUS SEEDACTIVE MOIETYMO892VI77K2
SUS SCROFA ARTERYACTIVE MOIETY63O327782Q2
SUS SCROFA PLACENTAACTIVE MOIETYC8CV8867O82
SUS SCROFA UMBILICAL CORDACTIVE MOIETY118OYG6W3H2
SUS SCROFA VEINACTIVE MOIETY2510RH3I892
TOBACCO LEAFACTIVE MOIETY6YR2608RSU2
VIPERA BERUS VENOMACTIVE MOIETY0ORO6NCA4M2
ALCOHOLINACTIVE INGREDIENT3K9958V90M2
WATERINACTIVE INGREDIENT059QF0KO0R2

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-040743742-0407-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Name, UNII, Kind table
NameUNIIKind
HORSE CHESTNUT3C18L6RJAZACTIB
LACTIC ACID, L-F9S9FFU82NACTIB
CLAVICEPS PURPUREA SCLEROTIUM01G9XEA93NACTIB
CUPRIC SULFATELRX7AJ16DTACTIM
MELILOTUS OFFICINALIS TOPGM6P02J2DXACTIB
SUS SCROFA PLACENTAC8CV8867O8ACTIB
SOLANUM NIGRUM WHOLE0FMD6WV47MACTIB
STROPHANTHUS HISPIDUS SEEDMO892VI77KACTIB
PRASTERONE459AG36T1BACTIB
QUERCETIN9IKM0I5T1EACTIB
RUTIN5G06TVY3R7ACTIB
SODIUM PYRUVATEPOD38AIF08ACTIB
SUS SCROFA VEIN2510RH3I89ACTIB
SUS SCROFA ARTERY63O327782QACTIB
SUS SCROFA UMBILICAL CORD118OYG6W3HACTIB
TOBACCO LEAF6YR2608RSUACTIB
VIPERA BERUS VENOM0ORO6NCA4MACTIB
BARIUM CARBONATE6P669D8HQ8ACTIB
LEAD IODIDEOTL90F2GLTACTIB
ASTRAGALUS EXSCAPUS WHOLE FLOWERING/FRUITING0II1G590JEACTIB
PROTEUS VULGARIS11T9HCO30OACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 59 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MSYRUP / ORAL21000 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / INTRAVESICAL7892 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MGEL / TOPICAL9971 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / RESPIRATORY (INHALATION)5 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MGEL / TRANSDERMAL7360 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MDROPS / ORAL210 mg/1mlExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / OPHTHALMIC0.5 %w/vExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / INTRAVENOUS99 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MDROPS / NASAL10 mg/1mlExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MAEROSOL, SPRAY / RESPIRATORY (INHALATION)35.75 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION, SOLUTION / INTRAVENOUS6405 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MGEL / DENTAL1.8 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MTABLET, DELAYED RELEASE / ORALNAExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION, CONCENTRATE / ORAL150.68 mg/1mlExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION / INTRAVENOUS92 %w/vExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MAEROSOL / NASAL20 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MPOWDER, FOR SOLUTION / TOPICAL40 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MGEL, METERED / TOPICAL541 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MAEROSOL, FOAM / TOPICAL4504 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MJELLY / VAGINALNAExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION / INTRAVASCULAR100 %v/vExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY / SUBLINGUAL397 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLOTION / TOPICAL25 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MPASTE / DENTAL1.8 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSUSPENSION / RECTAL0.35 %v/vExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE, EXTENDED RELEASE / ORAL8 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION, SOLUTION / INTRAMUSCULAR1000 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MAEROSOL, METERED / RESPIRATORY (INHALATION)26664 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / DENTAL12.8 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION / INTRAMUSCULAR1491 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MAEROSOL / TOPICAL561 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY / NASAL20 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MELIXIR / ORAL13675 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSHAMPOO / TOPICAL714 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE / ORAL882 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MGEL / RECTAL898 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION / SUBCUTANEOUS149 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / INTRAVENOUS400 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY / TRANSDERMAL90 %w/vExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION, CONCENTRATE / INTRAVENOUS4000 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / RESPIRATORY (INHALATION)0.08 %w/vExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSUSPENSION / ORAL681 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSWAB / TOPICAL2250 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / TOPICAL2445 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / INTRAMUSCULAR400 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / NASAL10 mg/1mlExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MGEL, METERED / TRANSDERMAL3675 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION, SOLUTION / SUBCUTANEOUS6.1 %v/vExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MMOUTHWASH / BUCCAL200 mg/1mlExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCONCENTRATE / ORAL198 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / ORAL6624 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION, EMULSION / INTRAVENOUS520 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCONCENTRATE / BUCCAL679 mg/1mlExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MAEROSOL, METERED / NASAL70 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / TRANSDERMAL49.37 %w/vExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY / TOPICAL3633 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MAEROSOL, SPRAY / TOPICAL561 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY, METERED / SUBLINGUAL29 mgExact identifier — unii candidate
59 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
fd32045d-ee46-46f9-8c10-46a7b1c5c9573615fdf9-bdc5-44ad-a9f3-cbd0ea87c4a52016-10-13WarningsExact identifier
spl id: fd32045d-ee46-46f9-8c10-46a7b1c5c957
spl set id: 3615fdf9-bdc5-44ad-a9f3-cbd0ea87c4a5

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.