Home FDA labels 136939aa-bd34-38a6-e063-6394a90abad0 Vitiligo openFDA label record# This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)
Brand name Vitiligo
Generic name ECHINACEA, IRIS VERSICOLOR, RUMEX CRISPUS, BERBERIS VULGARIS, BOVISTA, DOLICHOS PRURIENS, HURA BRASILIENSIS, HYDROCOTYLE ASIATICA, LYCOPODIUM CLAVATUM, MEZEREUM, RHUS TOXICODENDRON, SEPIA, TARAXACUM OFFICINALE, THUJA OCCIDENTALIS, URTICA URENS, ARSENICUM ALBUM
Manufacturer Newton Laboratories, Inc.
Product type HUMAN OTC DRUG
SPL set ID 136945e2-6f2a-a0df-e063-6294a90a994b
SPL ID 136939aa-bd34-38a6-e063-6394a90abad0
Version 1
Effective date 2024-03-11
Source export date 2026-10-12
Source partition 8
Source file https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:14:44 Harmonized routes table Harmonized routes ORAL
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 24 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Vitiligo openfda.brand_name generic name ECHINACEA, IRIS VERSICOLOR, RUMEX CRISPUS, BERBERIS VULGARIS, BOVISTA, DOLICHOS PRURIENS, HURA BRASILIENSIS, HYDROCOTYLE ASIATICA, LYCOPODIUM CLAVATUM, MEZEREUM, RHUS TOXICODENDRON, SEPIA, TARAXACUM OFFICINALE, THUJA OCCIDENTALIS, URTICA URENS, ARSENICUM ALBUM openfda.generic_name manufacturer name Newton Laboratories, Inc. openfda.manufacturer_name ndc package 55714-2592-1 openfda.package_ndc ndc product 55714-2592 openfda.product_ndc ndc11 package 55714259201 derived:openfda.package_ndc spl id 136939aa-bd34-38a6-e063-6394a90abad0 id spl set id 136945e2-6f2a-a0df-e063-6294a90a994b set_id unii K2A74U428F openfda.unii unii 3E271BSI0C openfda.unii unii X2N6E405GV openfda.unii unii 1TH8Q20J0U openfda.unii unii QDL83WN8C2 openfda.unii unii 39981FM375 openfda.unii unii 7M867G6T1U openfda.unii unii 1NT28V9397 openfda.unii unii 9N1RM2S62C openfda.unii unii IHN2NQ5OF9 openfda.unii unii 6IO182RP7A openfda.unii unii S7V92P67HO openfda.unii unii 4N9P6CC1DX openfda.unii unii 8UHN1I06UP openfda.unii unii X43D4L3DQC openfda.unii unii C88X29Y479 openfda.unii
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 1 matching rows.
warnings WARNINGS SECTION WARNINGS: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding , ask a doctor before use.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.