FDA.reportPublic FDA data

DysBio Plus

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2021-06-28
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:42:36

Label at a glance#

ProductDysBio Plus
Active ingredientECHINACEA ANGUSTIFOLIA, ALOE, COLCHICUM AUTUMNALE BULB, CITRULLUS COLOCYNTHIS FRUIT PULP, MERCURIC CHLORIDE, STRYCHNOS NUX-VOMICA SEED, ARSENIC TRIOXIDE, ACETIC ACID, QUININE SULFATE, VIBRIO CHOLERAE, PROTEUS VULGARIS, ESCHERICHIA COLI, HELICOBACTER PYLORI, BOTULINUM TOXIN TYPE A, SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR TYPHI, SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS, CLOSTRIDIUM DIFFICILE, BRUGIA MALAYI
Label structure9 sections

Dosage and administration

1-10 drops under the tongue, 3 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

Echinacea (Angustifolia) 3X, Aloe 6X, Colchicum Autumnale 8X, Colocynthis 8X, Mercurius Corrosivus 8X, Nux Vomica 8X, Arsenicum Album 8X, 12X, 30X, Aceticum Acidum 12X, Chininum Sulphuricum 12X, Cholera Nosode 12X, 30X, Proteus (Vulgaris) 16X, 30X, Colibacillinum Cum Natrum Muriaticum 30X, Helicobacter Pylori 30X, Botulinum 30X, 60X, Salmonella Typhi Nosode 33X, Morgan Gaertner 30C, Clostridium Difficile 30C, 45C, 60C, Brugia Malayi 39C, 60C, 200C.

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

For temporary relief of symptoms related to gastroenteritis including occasional diarrhea, stomach cramps, nausea, vomiting, flatulence and bloating.**

**These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

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, seek advice of 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, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

HOMEOPATHIC INDICATIONS:

INDICATIONS & USAGE SECTION

For temporary relief of symptoms related to gastroenteritis including occasional diarrhea, stomach cramps, nausea, vomiting, flatulence and bloating.**

**These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, 25% Ethanol.

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. By: Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070 www.desbio.com

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DESBIO

NDC 43742-1595-1

HOMEOPATHIC

DYSBIO

PLUS

1 FL OZ (30 ml)

Dysbio PlusDysbio Plus

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43742-1595DYSBIO PLUS (ECHINACEA (ANGUSTIFOLIA), ALOE, COLCHICUM AUTUMNALE, COLOCYNTHIS, MERCURIUS CORROSIVUS, NUX VOMICA, ARSENICUM ALBUM, ACETICUM ACIDUM, CHININUM SULPHURICUM, CHOLERA NOSODE, PROTEUS (VULGARIS), COLIBACILLINUM CUM NATRUM MURIATICUM, HELICOBACTER PYLORI, BOTULINUM, SALMONELLA TYPHI NOSODE, MORGAN GAERTNER, CLOSTRIDIUM DIFFICILE, BRUGIA MALAYI) LIQUID [DESERET BIOLOGICALS, INC.]3Legacy NDC20210629_b90f4a64-06d1-4f35-a700-46d64cd5aa93.zip

Products#

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

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-159543742-1595-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
ECHINACEA ANGUSTIFOLIAVB06AV5US8ACTIB
ALOEV5VD430YW9ACTIB
COLCHICUM AUTUMNALE BULB993QHL78E6ACTIB
CITRULLUS COLOCYNTHIS FRUIT PULP23H32AOH17ACTIB
MERCURIC CHLORIDE53GH7MZT1RACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
ARSENIC TRIOXIDES7V92P67HOACTIB
ACETIC ACIDQ40Q9N063PACTIB
QUININE SULFATEKF7Z0E0Q2BACTIB
VIBRIO CHOLERAE4M0784008HACTIB
PROTEUS VULGARIS11T9HCO30OACTIB
ESCHERICHIA COLI514B9K0L10ACTIB
HELICOBACTER PYLORIU09W5JOL3ZACTIB
BOTULINUM TOXIN TYPE AE211KPY694ACTIB
SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR TYPHI760T5R8B3OACTIB
SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDISY3V16D4PV4ACTIB
CLOSTRIDIUM DIFFICILEPJX89V9R6NACTIB
BRUGIA MALAYIV1NN02KTF0ACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML

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
77f20218-fa8a-4a9b-a642-a134ff0fbd9ab90f4a64-06d1-4f35-a700-46d64cd5aa932021-06-28WarningsExact identifier
spl id: 77f20218-fa8a-4a9b-a642-a134ff0fbd9a
spl set id: b90f4a64-06d1-4f35-a700-46d64cd5aa93

Reported adverse events (FAERS/openFDA)#

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