Calcarea Carbonica, Chenopodium Anthelminticum, Cocculus Indicus, Conium Maculatum, Nux Vomica, Phosphorus, Pulsatilla (vulgaris), Silicea
Generic Name: calcarea carbonica, chenopodium anthelminticum, cocculus indicus, conium maculatum, nux vomica, phosphorus, pulsatilla (vulgaris), silicea
Brand Names:
Dv Hp
INDICATIONS: For temporary relief of symptoms due to dizziness and light-headedness.
Overview
INDICATIONS: For temporary relief of symptoms due to dizziness and light-headedness.
Uses
INDICATIONS: For temporary relief of symptoms due to dizziness and light-headedness.
Dosage
DIRECTIONS: 10 drops orally, 3 times a day. Consult a physician for use in children under 12 years of age.
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.
Frequently Asked Questions
What is Calcarea Carbonica, Chenopodium Anthelminticum, Cocculus Indicus, Conium Maculatum, Nux Vomica, Phosphorus, Pulsatilla (vulgaris), Silicea used for?▼
INDICATIONS: For temporary relief of symptoms due to dizziness and light-headedness.
What are the important warnings for Calcarea Carbonica, Chenopodium Anthelminticum, Cocculus Indicus, Conium Maculatum, Nux Vomica, Phosphorus, Pulsatilla (vulgaris), Silicea?▼
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.
Related Medications
Manganum Metallicum
manganum metallicum
Chromium Metallicum
chromium metallicum
Standardized Chemical Allergen [EPC]
Metronidazole Hydrochloride
metronidazole hydrochloride
Manufactured by PFIZER. Dosage form: INJECTABLE. Route: INJECTION. Active ingredients: METRONIDAZOLE HYDROCHLORIDE (EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**). Application: NDA018353.
Medical Disclaimer
This drug information is for educational purposes only and should not replace professional medical advice. Drug information is sourced from the FDA National Drug Code Directory and Structured Product Labeling. Always consult with a healthcare provider before starting, stopping, or changing any medication.