Cortisol Phenolic
Cortisol Phenolic is an FDA drug label for the active ingredient HYDROCORTISONE manufactured by Energique, 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 20180913.
Generic: HYDROCORTISONE
Manufacturer: Energique, Inc.
Product Type: HUMAN OTC DRUG
Route: ORAL
Dosage Form:
NDC: 44911-0275
Application:
Effective: 20180913
Active Ingredients: ACTIVE INGREDIENT: (in each drop): 24.98% of Hydrocortisone 12X, 30X, 12C, 30C; 0.10 % of Hydrocortisone 6X.
Indications & Usage
INDICATIONS: May temporarily relieve symptoms associated with reactions to cortisol.** **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.
Dosage & Administration
DIRECTIONS: Adults and children 5 to 10 drops orally, 1 time daily or as otherwise directed by a health care professional. If symptoms persist, consult your health care professional. Consult a physician for use in children under 12 years of age.
Contraindications
Not available.
Warnings
WARNINGS: If pregnant or breast-feeding, 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.
Adverse Reactions
Not available.
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