Pulsatilla 200C
Pulsatilla 200C is an FDA drug label for the active ingredient PULSATILLA manufactured by Natural Creations, Inc 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 20181221.
- Generic name
- PULSATILLA
- Manufacturer
- Natural Creations, Inc
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 43406-0258
- Application
- N/A
- Label effective
- 20181221
Active ingredients
Indications & Usage
USES: Temporarily relieves moodiness, weepiness, &/or fear of abandoment.**
Dosage & Administration
DIRECTIONS: Adults & children above 12 years: 10 drops orally 3 times daily, or as directed by a health care professional.
Contraindications
Not available.
Warnings
WARNINGS: Consult a physician for use in children under 12 years of age. IF PREGNANT OR BREAST-FEEDING , ask a health care professional before use. KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away. Do not use if TAMPER EVIDENT seal is broken or missing.
Adverse Reactions
Not available.