Dosage & Administration
10-15 drops, 3-4 times a day in some water
Eugenia Jambosa Liquid
FDA Label NDC 85816-2222
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bm Private Limited for the product Eugenia Jambosa (NDC 85816-2222). 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 dosage & administration, otc - active ingredient, inactive ingredient, indications & usage, otc - purpose, otc - keep out of reach of children, warnings, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Active Ingredient
Arnica montana, baptisia, echinacea, eugenia jambosa, hepar shulph
Inactive Ingredient
ALCOHOL
Indications & Usage
For detail, please read the enclosed package (product information leaflet)
Otc - Purpose
For detail, please read the enclosed package (product information leaflet)
Otc - Keep Out Of Reach Of Children
Precautions/storage:
Keep away from children and store at cool and dry place.
Warnings
Precautions/storage:
Keep away from children and store at cool and dry place.
Package Label.Principal Display Panel
Entire package
* Please review the disclaimer below.
