Sulphur Remedy

Product NDC: 43742-0745
11-digit product format: 437420745
Labeler code: 43742
Product ID: 43742-0745_329b8913-d3b6-4d30-a089-215c3f2cdc49
Type: HUMAN OTC DRUG
Nonproprietary name: Sulphur, Asclepias Tuberosa, Bryonia, Dulcamara
Dosage form: LIQUID
Route: ORAL
Labeler: Deseret Biologicals, Inc.
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2016-05-04
Substance: SULFUR; ASCLEPIAS TUBEROSA ROOT; BRYONIA ALBA ROOT; SOLANUM DULCAMARA STEM
Active strength: 4; 6; 10; 10 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: Sulphur Remedy
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
SULFUR	4 [hp_X]/mL
ASCLEPIAS TUBEROSA ROOT	6 [hp_X]/mL
BRYONIA ALBA ROOT	10 [hp_X]/mL
SOLANUM DULCAMARA STEM	10 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
70FD1KFU70	Internal UNII lookup
1ZL82U5D18	Internal UNII lookup
T7J046YI2B	Internal UNII lookup
IR986LE7DF	Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
a77ef404-a836-4c3a-830f-bfe22127990f	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
43742-0745-1	Sulphur Remedy	30 mL in 1 BOTTLE, DROPPER	LIQUID	30		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
43742-0745	SULPHUR REMEDY (SULPHUR, ASCLEPIAS TUBEROSA, BRYONIA, DULCAMARA) LIQUID [DESERET BIOLOGICALS, INC.]	3	Current NDC, Legacy NDC, 1 package rows	20241025_a77ef404-a836-4c3a-830f-bfe22127990f.zip

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Sulphur Remedy	SULPHUR, ASCLEPIAS TUBEROSA, BRYONIA, DULCAMARA	Deseret Biologicals, Inc.	a77ef404-a836-4c3a-830f-bfe22127990f	2024-10-23	Warnings	Exact identifier ndc (product): 43742-0745

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
70FD1KFU70	SULFUR	7704-34-9	SULFUR
1ZL82U5D18	ASCLEPIAS TUBEROSA ROOT		ASCLEPIAS TUBEROSA ROOT
T7J046YI2B	BRYONIA ALBA ROOT		BRYONIA ALBA ROOT
IR986LE7DF	SOLANUM DULCAMARA STEM		SOLANUM DULCAMARA STEM

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
43742-0745-1	43742074501	30 mL in 1 BOTTLE, DROPPER (43742-0745-1)	30 ml	2016-05-04	0000-00-00	No	No	Current