The following Structured Product Label (SPL) was submitted to the FDA by Liddell Laboratories, Inc. for the product Eazol (NDC 50845-0131). 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 otc - active ingredient, otc - purpose, warnings, dosage & administration, inactive ingredient, otc - keep out of reach of children, indications & usage, otc - questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
ACTIVE INGREDIENTS: Aconitum napellus 200C, Arsenicum album 200C, Coffea cruda 200C, Euphorbium officinarum 4X, Gnaphalium polycephalum 3X, Hypericum perforatum 200C, Magnesia phosphorica 12X, Passiflora incarnata 1X, Ranunculus bulbosus 3X.
INDICATIONS: Provides natural temporary relief of minor aches and pains.
WARNINGS: If pregnant or breast feeding, seek the advice of a doctor before use.
Do not use if you have ever had an allergic reaction to this product or any of its ingredients.
Stop use and ask a doctor is symptoms persist, worsen or if new symptoms occur.
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 around neck of bottle is missing or broken.
DIRECTIONS: Adults and Children over 12: Spray twice under the tongue 3 times per day. Children under 12: Consult a doctor prior to use.
INACTIVE INGREDIENTS: Alcohol 20% v/v, Purified water.
KEEP OUT OF REACH OF CHILDREN. In case of overdose, get medical help or contact a Poison Control Center right away.
INDICATIONS: Provides natural temporary relief of minor aches and pains.
Distributed By:
Nutralogy
2049 North Lincoln Street
Burbank, CA 91504
Made in the USA
EAZOL
Natural Pain Relief
HOMEOPATHIC
1.0 FL OZ (30 ml)
Eazol (Mm1)
* Please review the disclaimer below.
