Sepia
SEPIA OFFICINALIS JUICE
ORAL
HUMAN OTC DRUG
Sepia is an FDA drug label for the active ingredient SEPIA OFFICINALIS JUICE 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
- SEPIA OFFICINALIS JUICE
- Manufacturer
- Boiron
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 0220-4646
- Application
- N/A
- Label effective
- 20231115
Active ingredients
Sepia 8X (**contains 0.443 mg of the active ingredient per pellet)
Indications & Usage
Bloating And Lower Back Pain During Menstruation*
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.