Jet Lag Relief
Jet Lag Relief is an FDA drug label for the active ingredient ANAMIRTA COCCULUS SEED, ARNICA MONTANA, STRYCHNOS NUX-VOMICA WHOLE manufactured by Laboratoires Boiron 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
- ANAMIRTA COCCULUS SEED, ARNICA MONTANA, STRYCHNOS NUX-VOMICA WHOLE
- Manufacturer
- Laboratoires Boiron
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 0220-9214
- Application
- N/A
- Label effective
- 20231004
Active ingredients
Indications & Usage
Uses* temporarily relieves symptoms such as: nausea stiffness muscle pain drowsiness
Dosage & Administration
Directions Keep packaging to save these directions for use. Adults and children 2 years of age and older: Dissolve 5 pellets of each medicine under the tongue: The day before traveling. Just before travel. At the onset of symptoms, then repeat 3 times a day until symptoms are relieved or as directed by a doctor. Children under 2 years of age: Ask a doctor.
Contraindications
Not available.
Warnings
Stop use and ask a doctor if symptoms persist for more than 3 days or worsen, new symptoms occur, or if redness or swelling if present. These could be signs of a serious condition. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
Adverse Reactions
Not available.