Drug Facts: Active Ingredients
Bryonia alba 30C HPUS, Rhus toxicodendron 200C HPUS
Dorspi 40 (number 552)
FDA Label NDC 69152-0552
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 Dorspi 40 (number 552) (NDC 69152-0552). 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 drug facts: 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
Sucrose, Lactose
Purpose
Relieves backache
Uses
Relieves backache
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: Take three pills daily. Leaving a gap of 30 minutes after any food or as advised by your physician.
Manufactured By
Paramesh Banerji Life Sciences, LLC.
North Brunswick, NJ 08902, USA.
Tel: +1-732-743-5936
Email: [email protected]
Principal Display Panel
NDC: 69152-0552-1
Dorspi 40
Number 552
Homeopathic Medicine
Relieves backache
96 Pills (Approx.)
Product of USA
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