Sulfur
Sulfur is an FDA drug label for the active ingredient SULFUR manufactured by True Botanica, LLC 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 20230602.
- Generic name
- SULFUR
- Manufacturer
- True Botanica, LLC
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 53645-1200
- Application
- N/A
- Label effective
- 20230602
Active ingredients
Indications & Usage
Use: For temporary relief of skin eruptions, insomnia. May also be used for standard homeopathic indications or as directed by your physician.
Dosage & Administration
Directions for Use: Place globules under tongue for 30 seconds. Adults~3-5 globules 3 times a day. Children 2-12 years ~ 1-3 globules 3 times a day. Under 2 years, consult your doctor. Use until symptoms are relieved or as directed by your health care provider.
Contraindications
Not available.
Warnings
Warnings: Consult your health care provider if symptoms persist more than 5 days or worsen.
Adverse Reactions
Not available.