Active Ingredients
Lepidolite 6X, 8X, 12X, 30X
Lepidolite Liquid
FDA Label NDC 63083-8130
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Professional Complementary Health Formulas for the product Lepidolite (NDC 63083-8130). 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, questions, indications, otc - purpose, warnings, otc - keep out of reach of children, otc - pregnancy or breast feeding, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Questions
Professional Formulas
PO Box 2034 Lake Oswego, OR 97035
Indications
Temporarily relieves hopelessness, worry, impatience, low self-esteem, or mental/emotional imbalance.*
Otc - Purpose
*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Warnings
In case of overdose, get medical help or contact a poison control center right away.
Otc - Keep Out Of Reach Of Children
Keep out of the reach of children.
Otc - Pregnancy Or Breast Feeding
If pregnant or breastfeeding, ask a healthcare professional before use.
Directions
Place drops under tongue 30 minutes before/after meals. Adults and children 12 years and over: Take 10 drops up to 3 times per day. Consult a physician for use in children under 12 years of age.
Other Information
Tamper resistant. If seal is broken, do not use. After opening, close container tightly and store at room temperature away from heat.
Inactive Ingredients
20% ethanol, purified water.
Label
Est 1985
Professional Formulas
Complementary Health
Lepidolite
Homeopathic Remedy
2 FL. OZ. (59 mL)
Label Image (Ulep Thumb)
* Please review the disclaimer below.
