Sulphur
SULFUR
ORAL
HUMAN OTC DRUG
Sulphur is an FDA drug label for the active ingredient SULFUR manufactured by Boiron administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231115.
- Generic name
- SULFUR
- Manufacturer
- Boiron
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 0220-4829
- Application
- N/A
- Label effective
- 20231115
Active ingredients
Sulphur 15C (**contains 0.443 mg of the active ingredient per pellet)
Indications & Usage
Skin Rash Worsened By Heat And Water*
Dosage & Administration
Adults and children: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.
Contraindications
Not available.
Warnings
Not available.
Adverse Reactions
Not available.