Sulphur Remedy

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2024-10-23
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:28:22

Label at a glance#

ProductSulphur Remedy
Active ingredientSULFUR, ASCLEPIAS TUBEROSA ROOT, BRYONIA ALBA ROOT, SOLANUM DULCAMARA STEM
Label structure9 sections

Indications and uses

• For the temporary relief of symptoms including: • headache • fever • muscle aches • skin inflammation These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

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

 Asclepias Tuberosa 6X, 10X, 30X, Bryonia (Alba) 10X, 30X, Dulcamara 10X, 30X, Sulphur 4X, 10X.

PURPOSE:

OTC - PURPOSE SECTION

Asclepias Tuberosa - Headache, Bryonia (Alba) - Fever, Dulcamara - Muscle Aches, Sulphur - Skin Inflammation

USES:

INDICATIONS & USAGE SECTION

• For the temporary relief of symptoms including:

• headache • fever • muscle aches • skin inflammation

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

WARNINGS:

WARNINGS SECTION

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

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

Tamper Evident: 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.

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

800-827-8204

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DesBio

Sulphur Remedy

Homeopathic

NDC 43742-0745-1

1 FL OZ (30 ml)

Sulphur RemedySulphur Remedy

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43742-0745-1Sulphur Remedy30 mL in 1 BOTTLE, DROPPERLIQUID303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43742-0745SULPHUR REMEDY (SULPHUR, ASCLEPIAS TUBEROSA, BRYONIA, DULCAMARA) LIQUID [DESERET BIOLOGICALS, INC.]3Current NDC, Legacy NDC, 1 package rows20241025_a77ef404-a836-4c3a-830f-bfe22127990f.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-074543742-0745-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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
Sulphur RemedySULPHUR, ASCLEPIAS TUBEROSA, BRYONIA, DULCAMARADeseret Biologicals, Inc.a77ef404-a836-4c3a-830f-bfe22127990f2024-10-23WarningsExact identifier
ndc (package): 43742-0745-1
ndc (product): 43742-0745
ndc11 (package): 43742074501
spl id: 329b8913-d3b6-4d30-a089-215c3f2cdc49
spl set id: a77ef404-a836-4c3a-830f-bfe22127990f

Reported adverse events (FAERS/openFDA)#

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