Active Ingredients
Ignatia amara HPUS
6X, 12X, 30X, 6C, 9C, 12C, 15C, 30C, 200CK, 1M, 10M, 50M, 1CM
Ignatia Amara Pellet
FDA Label NDC 0220-2613
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Boiron for the product Ignatia Amara (NDC 0220-2613). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients, use, stop use and ask a doctor if, if pregnant or breast-feeding,, directions, other information, inactive ingredients, questions, comments?, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Use
Apprehension, hypersensitivity to stress*
Stop Use And Ask A Doctor If
symptoms persist for more than 3 days or worsen.
If Pregnant Or Breast-Feeding,
ask a health professional before use.
Directions
5 pellets 3 times a day until symptoms are relieved.
Other Information
Do not use if pellet dispenser seal is broken.
contains approx. 80 pellets
Inactive Ingredients
lactose, sucrose
Questions, Comments?
1-800-BOIRON-1
Newtown Square, PA 19073-3267
[email protected]
*
These "Uses" have not been evaluated by the FDA.
* Please review the disclaimer below.
