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
ASCLEPIAS TUBEROSA ROOT; BRYONIA ALBA ROOT; SOLANUM DULCAMARA STEM; SULFUR
Active strength
6; 10; 10; 4 [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

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ASCLEPIAS TUBEROSA ROOT6 [hp_X]/mL
BRYONIA ALBA ROOT10 [hp_X]/mL
SOLANUM DULCAMARA STEM10 [hp_X]/mL
SULFUR4 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii1ZL82U5D18, T7J046YI2B, IR986LE7DF, 70FD1KFU70

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

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43742-0745-14374207450130 mL in 1 BOTTLE, DROPPER (43742-0745-1) 30 ml2016-05-040000-00-00NoNoCurrent