Home FDA labels 4d45ca3f-33e3-455c-89c4-1c9a4025a617 Skin Liquescence 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 Skin Liquescence
Generic name ANGELICA ARCHANGELICA, BERBERIS AQUIFOLIUM, BERBERIS VULGARIS, EQUISETUM ARVENSE, GERANIUM MACULATUM, MYRRHA, IRIS VERSICOLOR, THUJA OCCIDENTALIS, NUX VOMICA, HYPERICUM PERFORATUM, HUMAN GROWTH HORMONE (HGH), MERCURIUS SOLUBILIS, PETROLEUM, GRAPHITES
Manufacturer Nutritional Specialties, Inc.
Product type HUMAN OTC DRUG
SPL set ID dce5fdc8-a3d5-482f-bc15-2ca1e7789e0f
SPL ID 4d45ca3f-33e3-455c-89c4-1c9a4025a617
Version 2
Effective date 2025-05-06
Source export date 2026-10-12
Source partition 14
Source file https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/acb9b4700b9af1bdda1c389c7b35bfe38fd6d1a62aa48d17832812be4029b84f/drug-label-0014-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 03:12:43 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 · 22 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Skin Liquescence openfda.brand_name generic name ANGELICA ARCHANGELICA, BERBERIS AQUIFOLIUM, BERBERIS VULGARIS, EQUISETUM ARVENSE, GERANIUM MACULATUM, MYRRHA, IRIS VERSICOLOR, THUJA OCCIDENTALIS, NUX VOMICA, HYPERICUM PERFORATUM, HUMAN GROWTH HORMONE (HGH), MERCURIUS SOLUBILIS, PETROLEUM, GRAPHITES openfda.generic_name manufacturer name Nutritional Specialties, Inc. openfda.manufacturer_name ndc package 83027-0054-1 openfda.package_ndc ndc product 83027-0054 openfda.product_ndc ndc11 package 83027005401 derived:openfda.package_ndc spl id 4d45ca3f-33e3-455c-89c4-1c9a4025a617 id spl set id dce5fdc8-a3d5-482f-bc15-2ca1e7789e0f set_id unii XK4IUX8MNB openfda.unii unii 269XH13919 openfda.unii unii 324Y4038G2 openfda.unii unii 4QQN74LH4O openfda.unii unii VZJ9F3C3SB openfda.unii unii 1TH8Q20J0U openfda.unii unii 1NT28V9397 openfda.unii unii 93IXI5B6OJ openfda.unii unii DTN01M69SN openfda.unii unii NQX9KB6PCL openfda.unii unii X43D4L3DQC openfda.unii unii 1C89KKC04E openfda.unii unii 1DP6Y6B65Z openfda.unii unii JC71GJ1F3L 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: If pregnant or breast-feeding, ask a health professional before use. In case of overdose, get medical help or contact a Poison Control Center right away. If condition worsens, seek medical attention. KEEP OUT OF REACH OF CHILDREN Do not use if tamper evident seal is broken or missing. Store in a cool place after opening
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.