United States · FDA National Drug Code directory
Sulphur Remedy
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 43742-0745_329b8913-d3b6-4d30-a089-215c3f2cdc49
- Product NDC
- 43742-0745
- Form
- LIQUID
- Composition / generic term
- Sulphur, Asclepias Tuberosa, Bryonia, Dulcamara
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 20160504
- Source listing expiry
- 20261231
Source-listed ingredients
- 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
These values do not establish equivalence or a dose recommendation.
Packages
- 30 mL in 1 BOTTLE, DROPPER (43742-0745-1) · 43742-0745-1
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →