Home NDC 70957-0020-1 Vitiligo Organics
Product NDC 70957-0020
Requested package NDC 70957-0020-1
11-digit product format 709570020
Labeler code 70957
Product ID 70957-0020_415c57c5-9433-30ce-e063-6394a90acc03
Type HUMAN OTC DRUG
Nonproprietary name Cullen corylifolium whole plant, Berberis vulgaris root bark, Nigella sativa seed, Organic coconut oil
Dosage form OINTMENT
Route TOPICAL
Labeler Organic Care Australia Pty LTD
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2016-09-07
Substance BERBERIS VULGARIS ROOT BARK; CULLEN CORYLIFOLIUM WHOLE; NIGELLA SATIVA SEED
Active strength 83; 83; 83 mg/125mL; mg/125mL; mg/125mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Vitiligo Organics
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CULLEN CORYLIFOLIUM WHOLE 83 mg/125mL NIGELLA SATIVA SEED 83 mg/125mL BERBERIS VULGARIS ROOT BARK 83 mg/125mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination M8Z0AK5HFO Internal UNII lookup 4LVZ0Z0ITT Internal UNII lookup 1TH8Q20J0U Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70957-0020-1 Vitiligo Organics 125 mL in 1 BOTTLE OINTMENT 125 10 70957-0020-2 Vitiligo Organics 250 mL in 1 BOTTLE OINTMENT 250 10
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70957-0020 VITILIGO ORGANICS (CULLEN CORYLIFOLIUM WHOLE PLANT, BERBERIS VULGARIS ROOT BARK, NIGELLA SATIVA SEED, ORGANIC COCONUT OIL) OINTMENT [ORGANIC CARE AUSTRALIA PTY LTD] 9 Current NDC, Legacy NDC, 2 package rows 20250326_3bebd5f6-e5c1-0501-e054-00144ff8d46c.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 70957-0020-1 70957002001 125 mL in 1 BOTTLE (70957-0020-1) 125 ml 2016-09-07 0000-00-00 No No Current