Arthri-Joint T008
Arthri-Joint T008 is an FDA drug label for the active ingredient APIS MELLIFICA, BRYONIA (ALBA), CAUSTICUM, COLCHICUM AUTUMNALE, KALI CARBONICUM, KALMIA LATIFOLIA, LEDUM PALUSTRE, PULSATILLA (VULGARIS), RHODODENDRON CHRYSANTHUM, RHUS TOX manufactured by Guangzhou Renuma Medical Systems Co., Ltd 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 20171023.
- Generic name
- APIS MELLIFICA, BRYONIA (ALBA), CAUSTICUM, COLCHICUM AUTUMNALE, KALI CARBONICUM, KALMIA LATIFOLIA, LEDUM PALUSTRE, PULSATILLA (VULGARIS), RHODODENDRON CHRYSANTHUM, RHUS TOX
- Manufacturer
- Guangzhou Renuma Medical Systems Co., Ltd
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 71742-0002
- Application
- N/A
- Label effective
- 20171023
Active ingredients
Indications & Usage
INDICATIONS: May temporarily relieve symptoms due to minor joint inflammation and swelling.
Dosage & Administration
DIRECTIONS: Adults and children 5 to 10 drops orally, 1 to 2 times daily or as otherwise directed by a health care professional. If symptoms persist, 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 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.