Dosage and administration
Adults and children over 12: Spray twice under the tongue every 30 minutes until symptoms are relieved. Children 12 and under: Consult a doctor prior to use.
Adults and children over 12: Spray twice under the tongue every 30 minutes until symptoms are relieved. Children 12 and under: Consult a doctor prior to use.
Aconitum Napellus 200C, Arnica Montana 3X, Arsenicum Album 200C, Bellis Perennis 3X, Cartilago Suis 6X, Causticum 200X, Chamomilla 3X, Coffea Cruda 200C, Euphorbium Officinarum 6X, Gnaphalium Polycephalum 3X, Hypericum Perforatum 200C, Magnesia Phosphorica 12X, Passiflora Incarnata 1X, Pyrogenium 200C, Ranunculus Bulbosus 3X, Symphytum Officinale 6X.
May temporarily relieve minor aches and pains.**
**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.
If symptoms persist, consult a doctor.
If pregnant or breast feeding, ask a doctor before use.
Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.
Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.
Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.
Adults and children over 12: Spray twice under the tongue every 30 minutes until symptoms are relieved.
Children 12 and under: Consult a doctor prior to use.
May temporarily relieve minor aches and pains.**
**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.
Organic alcohol 20% v/v, Purified water.
ORAL SPRAYS
LIDDELL
LABORATORIES
EST. 1994
39 Pn
HOMEOPATHIC
1.0 FL. OZ. (30ml)
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 50845-0233 | 50845-0233-1 |
Every source-derived ingredient row is available through these pages.
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 755c5983-3d1b-4e5f-9653-9056efa925bd | a04897b4-8461-4eb2-a689-16df0dc2f609 | 2019-02-05 | Warnings | 755c5983-3d1b-4e5f-9653-9056efa925bd a04897b4-8461-4eb2-a689-16df0dc2f609 |
Adverse event summaries are temporarily unavailable. Other product information remains available.