Uric Acid Balancer
Uric Acid Balancer is an FDA drug label for the active ingredient DULCAMARA, LEDUM PALUSTRE, ARNICA MONTANA, BENZOICUM ACIDUM, BRYONIA (ALBA), COLCHICUM AUTUMNALE, LITHIUM CARBONICUM, NATRUM PHOSPHORICUM, URTICA URENS, FORMICA RUFA, LYCOPODIUM CLAVATUM 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 20231004.
- Generic name
- DULCAMARA, LEDUM PALUSTRE, ARNICA MONTANA, BENZOICUM ACIDUM, BRYONIA (ALBA), COLCHICUM AUTUMNALE, LITHIUM CARBONICUM, NATRUM PHOSPHORICUM, URTICA URENS, FORMICA RUFA, LYCOPODIUM CLAVATUM
- Manufacturer
- Nutritional Specialties, Inc.
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 83027-0112
- Application
- N/A
- Label effective
- 20231004
Active ingredients
Indications & Usage
INDICATIONS: Aids in balancing uric acid levels.† †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.