Home FDA labels c1d54119-c619-4175-b4d8-f1fbddd4e5bc Gallcill 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 Gallcill
Generic name CHELIDONIUM MAJUS, BERBERIS AQUIFOLIUM, BERBERIS VULGARIS, DIOSCOREA VILLOSA, CALCAREA SULPHURICA, CUPRESSUS LAWSONIANA, HEPAR SULPHURICA CALCAREUM, CHOLESTERINUM, FEL TAURI, LYCOPODIUM CLAVATUM, MAGNESIA SULPHURICA
Manufacturer Nucleic Products, LLC
Product type HUMAN OTC DRUG
SPL set ID faf3ac96-b744-448d-b41a-8370b3ef3c0c
SPL ID c1d54119-c619-4175-b4d8-f1fbddd4e5bc
Version 4
Effective date 2025-12-03
Source export date 2026-10-12
Source partition 10
Source file https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:29:12 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 · 19 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Gallcill openfda.brand_name generic name CHELIDONIUM MAJUS, BERBERIS AQUIFOLIUM, BERBERIS VULGARIS, DIOSCOREA VILLOSA, CALCAREA SULPHURICA, CUPRESSUS LAWSONIANA, HEPAR SULPHURICA CALCAREUM, CHOLESTERINUM, FEL TAURI, LYCOPODIUM CLAVATUM, MAGNESIA SULPHURICA openfda.generic_name manufacturer name Nucleic Products, LLC openfda.manufacturer_name ndc package 75053-0006-1 openfda.package_ndc ndc product 75053-0006 openfda.product_ndc ndc11 package 75053000601 derived:openfda.package_ndc spl id c1d54119-c619-4175-b4d8-f1fbddd4e5bc id spl set id faf3ac96-b744-448d-b41a-8370b3ef3c0c set_id unii IWY3IWX2G8 openfda.unii unii E934B3V59H openfda.unii unii 7E889U5RNN openfda.unii unii ET3651ZLOU openfda.unii unii VZJ9F3C3SB openfda.unii unii 1TH8Q20J0U openfda.unii unii Q8HN1T482A openfda.unii unii 97C5T2UQ7J openfda.unii unii SK47B8698T openfda.unii unii C88X29Y479 openfda.unii unii 1MBW07J51Q 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: As with any drug, ask a doctor before use if pregnant or nursing. Consult a physician if: symptoms persist for more than 7 days or worsen. Keep this and all medications out of the reach of children. In case of accidental overdose, contact a medical professional or a Poison Control Center immediately. Do not use if seal is broken or missing. This Product does not contain sugar, starch, preservatives, artificial flavors or additives, and no wheat, gluten, soy, or milk derivatives.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.