Active Ingredients
Artemisia vulgaris 1X HPUS
Artemisia Vulgaris 1x
FDA Label NDC 69152-1574
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Paramesh Banerji Life Sciences Llc for the product Artemisia Vulgaris 1x (NDC 69152-1574). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients, inactive ingredients, purpose, uses, warnings, keep out of reach of children, direction, manufactured by, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredients
Ethyl alcohol, Water
Purpose
Epilepsy related unconsciousness
Uses
Epilepsy related unconsciousness
Warnings
If pregnant or breast feeding ask a health professional before use.
Keep Out Of Reach Of Children
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
Direction
Adult or child: Five drops in 3 tea spoons of water, leaving a gap of 30 minutes from any food or as advised by your physician.
Manufactured By
Paramesh Banerji Life Sciences, LLC
220 North Center Drive
North Brunswick, NJ 08902, USA
Product of USA
Tel: +1-732-743-5936
Principal Display Panel
Homeopathic Product
Artemisia vulgaris 1X
Homeopathic Product
Artemisia vulgaris 1X HPUS
Epilepsy related unconsciousness
Quantity
8 mL
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