VITILIGO ORGANICS- cullen corylifolium whole plant, berberis vulgaris root bark, nigella sativa seed, organic coconut oil ointment

Vitiligo Organics by

Drug Labeling and Warnings

Vitiligo Organics by is a Homeopathic medication manufactured, distributed, or labeled by Organic Care Australia Pty LTD, FERNGROVE PHARMACEUTICALS AUSTRALIA PTY LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Actives 

Each 1g contains:

Cullen corylifolium whole plant...83mg

Berberis vulgaris root bark...83mg

Nigella sativa seed...83mg

Purpose

For repigmentation of skin

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

VITILIGO ORGANICS 
cullen corylifolium whole plant, berberis vulgaris root bark, nigella sativa seed, organic coconut oil ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70957-0020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U)	BERBERIS VULGARIS ROOT BARK	83 mg  in 125 mL
CULLEN CORYLIFOLIUM WHOLE (UNII: M8Z0AK5HFO) (CULLEN CORYLIFOLIUM WHOLE - UNII:M8Z0AK5HFO)	CULLEN CORYLIFOLIUM WHOLE	83 mg  in 125 mL
NIGELLA SATIVA SEED (UNII: 4LVZ0Z0ITT) (NIGELLA SATIVA SEED - UNII:4LVZ0Z0ITT)	NIGELLA SATIVA SEED	83 mg  in 125 mL

Inactive Ingredients
Ingredient Name	Strength
COCONUT OIL (UNII: Q9L0O73W7L)	752 mg  in 125 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70957-0020-1	125 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/07/2016
2	NDC: 70957-0020-2	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/07/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		09/07/2016

Labeler - Organic Care Australia Pty LTD (757612684)

Registrant - Organic Care Australia Pty LTD (757612684)

Establishment
Name	Address	ID/FEI	Business Operations
Ultra Mix (Aust) Pty Ltd		752254649	manufacture(70957-0020)