Sinus Relief Formula

PULSATILLA (PRATENSIS), SINAPIS NIGRA, LUFFA OPERCULATA, EUPHORBIUM OFFICINARUM, GUAIACUM, MERCURIUS SULPHURATUS RUBER ORAL HUMAN OTC DRUG

Sinus Relief Formula is an FDA drug label for the active ingredient PULSATILLA (PRATENSIS), SINAPIS NIGRA, LUFFA OPERCULATA, EUPHORBIUM OFFICINARUM, GUAIACUM, MERCURIUS SULPHURATUS RUBER manufactured by Nutritional Specialties, 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 20230928.

Generic name
PULSATILLA (PRATENSIS), SINAPIS NIGRA, LUFFA OPERCULATA, EUPHORBIUM OFFICINARUM, GUAIACUM, MERCURIUS SULPHURATUS RUBER
Manufacturer
Nutritional Specialties, Inc.
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
83027-0105
Application
N/A
Label effective
20230928

Active ingredients

ACTIVE INGREDIENTS: Pulsatilla 4X, Sinapis Nigra 4X, Luffa Operculata 5X, Euphorbium Officinarum 8X, Guaiacum 12X, Mercurius Sulphuratus Ruber 12X.

Indications & Usage

INDICATIONS: Aids in temporary relief of sinus congestion and irritation.† †Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Dosage & Administration

DIRECTIONS: Adults: 2 to 3 sprays orally, three times daily. Children under twelve one half adult dosage. Do not take within 15 minutes of consuming food, beverage or brushing teeth. Consult a physician for use in children under 12 years of age.

Contraindications

Not available.

Warnings

WARNINGS: Professional Use Only If pregnant or breast-feeding, ask a health professional before use. In case of overdose, get medical help or contact a Poison Control Center right away. If condition worsens, seek medical attention. KEEP OUT OF REACH OF CHILDREN Do not use if tamper evident seal is broken or missing. Store in a cool place after opening

Adverse Reactions

Not available.