FDA.reportPublic FDA data

Dysbio Plus

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2024-02-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:26:00

Label at a glance#

ProductDysbio Plus
Active ingredientECHINACEA ANGUSTIFOLIA WHOLE, 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, CLOSTRIDIUM BOTULINUM, SALMONELLA ENTERICA 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 3X, Aloe 7X, Colchicum Autumnale 8X, Colocynthis 8X, Mercurius Corrosivus 8X, Nux Vomica 8X, Arsenicum Album 8X, 12X, 30X, Aceticum Acidum 12X, Chininum Sulphuricum 12X, Cholera Nosode 16X, 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.

PURPOSE:

OTC - PURPOSE SECTION

For temporary relief of symptoms related of 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, 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

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.

INDICATIONS

INDICATIONS & USAGE SECTION

For temporary relief of symptoms related of 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 43742-2084-1

HOMEOPATHIC

DYSBIO

PLUS

1 FL OZ (30 ml)

DYSBIO PLUSDYSBIO PLUS

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506
48747306-602a-42cc-957b-5b0c69158eeeProduct name120180604
22bca8fc-c2b1-897d-b515-117a7522ccaeProduct name320150731
db5ebcdb-b6ae-21cd-4dc5-76cd84b5578bProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43742-2084-1Dysbio Plus30 mL in 1 BOTTLE, DROPPERLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43742-2084DYSBIO 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.]2Current NDC, 1 package rows20240208_974f23e5-9062-42c1-9df3-12168edee141.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
43742-208443742-2084-1

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 ANGUSTIFOLIA WHOLEVB06AV5US8ACTIB
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
CLOSTRIDIUM BOTULINUM0296055VE0ACTIB
SALMONELLA ENTERICA 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
Dysbio PlusECHINACEA (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 MALAYIDeseret Biologicals, Inc.974f23e5-9062-42c1-9df3-12168edee1412024-02-07WarningsExact identifier
ndc (package): 43742-2084-1
ndc (product): 43742-2084
ndc11 (package): 43742208401
spl id: 7287390d-e064-4ee5-b8d9-9d72d33f6a8d
spl set id: 974f23e5-9062-42c1-9df3-12168edee141

Reported adverse events (FAERS/openFDA)#

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