FDA Label for Pulsatilla
View Indications, Usage & Precautions
Pulsatilla Product Label
The following document was submitted to the FDA by the labeler of this product Energique, Inc.. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredient:
(in each drop): 100% of Pulsatilla (Pratensis) 200C.
Indications:
May temporarily relieve menstrual pain, irregularity, and moodiness, especially with shifting, changeable symptoms.
May temporarily relieve menstrual pain, irregularity, and moodiness, especially with shifting, changeable symptoms.
Warnings:
If pregnant or breastfeeding, ask a health professional before use.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
Do not use if tamper evident seal is broken or missing.
Store in a cool, dry place.
Keep Out Of Reach Of Children:
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
Directions:
Adults and children 5 to 10 drops orally, 1 time daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.
Inactive Ingredients:
Demineralized water, 20% Ethanol
Questions:
Dist. by Energique, Inc.
201 Apple Blvd.
Woodbine, IA 51579 800.868.8078
Package Label Display:
ENERGIQUE
SINCE 1987
PULSATILLA
200C
1 fl. oz. (30 ml)
* Please review the disclaimer below.