Dopamine

DOPAMINE HYDROCHLORIDE ORAL HUMAN OTC DRUG

Dopamine is an FDA drug label for the active ingredient DOPAMINE HYDROCHLORIDE manufactured by BioActive Nutritional 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 20160816.

Generic name
DOPAMINE HYDROCHLORIDE
Manufacturer
BioActive Nutritional
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
43857-0412
Application
N/A
Label effective
20160816

Active ingredients

ACTIVE INGREDIENT: Dopamine Hydrochloride 6X.

Indications & Usage

INDICATIONS: For temporary relief of anxiety, hives, hay fever, chest congestion with constriction, ear pressure, neck and shoulder pain.

Dosage & Administration

DIRECTIONS: 10 drops orally, 3 times a day. 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 care 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 cool, dry place.

Adverse Reactions

Not available.

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