Norepinephrine
Norepinephrine is an FDA drug label for the active ingredient NOREPINEPHRINE (BITARTRATE) manufactured by Deseret Biologicals, 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 20230111.
- Generic name
- NOREPINEPHRINE (BITARTRATE)
- Manufacturer
- Deseret Biologicals, Inc.
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 43742-1489
- Application
- N/A
- Label effective
- 20230111
Active ingredients
Indications & Usage
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to Norepinephrine sensitivity including rashes, hives, Premenstrual Syndrome, and headache.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Dosage & Administration
DIRECTIONS: 1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.
Contraindications
Not available.
Warnings
WARNINGS: Keep out of reach of children. In case of overdose, contact physician or a Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use. Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.
Adverse Reactions
Not available.