Norepinephrine Phenolic

Norepinephrine Phenolic is an FDA drug label for the active ingredient NOREPINEPHRINE (BITARTRATE) 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 20230412.

Generic: NOREPINEPHRINE (BITARTRATE)

Manufacturer: Energique, Inc.

Product Type: HUMAN OTC DRUG

Route: ORAL

Dosage Form:

NDC: 44911-0669

Application:

Effective: 20230412

Active Ingredients: ACTIVE INGREDIENT: (in each drop): 25% of Norepinephrine 6X, 12X, 30X; 12.50% of Norepinephrine 12C, 30C.

Indications & Usage

INDICATIONS: May temporarily relieve symptoms associated with reactions to norepinephrine.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

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 for more than 7 days, 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