Otc - Active Ingredient
Crataegus Oxyacantha, Passiflora Incarnata, Rauwolfia Serpentina, Kali Bromatum
Rolfia
FDA Label NDC 69825-007
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Adven Biotech Private Limited for the product Rolfia (NDC 69825-007). 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 otc - active ingredient, dosage & administration, warnings:, otc - purpose, uses:, inactive ingredient, otc - do not use, 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
Dosage & Administration
Adults: Take 2 tablets with water every 8 hours.
Children under 18 years: Please consult physician.
Warnings:
If symptons persist or worsen, a physician should be consulted. Keep out of reach of children. Do not use, if known sentivity to any of its ingredients exists. Replace cap tightly. If pregnant or breast feeding, ask a health care professional before use.
Otc - Purpose
Tones up the Heart Muscle, Controls hypertension. Decrease Blood Pressure
Uses:
Normalizes high blood pressure, conrols hypertension, tones up the heart muscle, treats arteriosclerosis and related symptoms like sleeplessness, irritability.
Inactive Ingredient
Sugar of milk
Otc - Do Not Use
Do not use if neck wrap or foil inner seal is broken or missing. Protect from moisture, direct sunlight and heat.
Package Label.Principal Display Panel
Rolfia Tablets Label (Rolfiatablets)
* Please review the disclaimer below.
