Actives
Each 1g contains:
Cullen corylifolium whole plant...83mg
Berberis vulgaris root bark...83mg
Nigella sativa seed...83mg
Vitiligo Organics Ointment
FDA Label NDC 70957-0020
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Organic Care Australia Pty Ltd for the product Vitiligo Organics (NDC 70957-0020). 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 actives, purpose, otc - keep out of reach of children, warnings, directions, usage, inactives, 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
Purpose
For repigmentation of skin
Otc - Keep Out Of Reach Of Children
Keep out of reach of children
Warnings
• For external use only
• If symptoms persist consult your healthcare practitioner
• Store below 86 oF
Directions
Clean the affected area Apply generously and massage into the skin every day and night before bed Leave it on without rinsing for 8-10 hours Lotion solidifies in cold weather.
Immerse bottle in a warm bowl of water until liquefied Shake well before use
Usage
Homeopathic remedy that helps in pigmentation of skin affected by vitiligo.
Inactives
Coconut Oil
Package Label.Principal Display Panel
Voau_250ml_2016_v1 (Voau 125ml)
Voau_125ml_2016_v1 (Voau 250ml)
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