Home FDA labels 0906a66d-7256-a993-e063-6394a90a7150 Mineffect hangover relief 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 Mineffect hangover relief
Generic name ALUMINA SILICATA, CALCAREA SILICATA, SILICEA, FERRUM METALLICUM, FERRUM PHOSPHORICUM, FERRUM MURIATICUM, SULPHUR, PHOSPHORUS
Manufacturer Kadesh Incoporation Co,Ltd
Product type HUMAN OTC DRUG
SPL set ID c9821e87-1e8d-48ab-8821-32e7e660309a
SPL ID 0906a66d-7256-a993-e063-6394a90a7150
Version 2
Effective date 2023-10-31
Source export date 2026-10-30
Source partition 3
Source file https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-30/e1583c3c823c7746dc6fefae78ac97d01bb558f7b0936fc3b7d2e673d3319207/drug-label-0003-of-0014.json.zip
Source manifest SHA-256 b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run 20261102T182004Z
Imported at 2026-11-02 18:35:50 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 · 16 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Mineffect hangover relief openfda.brand_name generic name ALUMINA SILICATA, CALCAREA SILICATA, SILICEA, FERRUM METALLICUM, FERRUM PHOSPHORICUM, FERRUM MURIATICUM, SULPHUR, PHOSPHORUS openfda.generic_name manufacturer name Kadesh Incoporation Co,Ltd openfda.manufacturer_name ndc package 81488-007-60 openfda.package_ndc ndc product 81488-007 openfda.product_ndc ndc11 package 81488000760 derived:openfda.package_ndc spl id 0906a66d-7256-a993-e063-6394a90a7150 id spl set id c9821e87-1e8d-48ab-8821-32e7e660309a set_id unii 27YLU75U4W openfda.unii unii ETJ7Z6XBU4 openfda.unii unii 0I2XIN602U openfda.unii unii 91GQH8I5F7 openfda.unii unii 24H4NWX5CO openfda.unii unii 70FD1KFU70 openfda.unii unii E1UOL152H7 openfda.unii unii S4255P4G5M 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 Do not Use *If the tamper resistant label is broken When using this product *To avoid contamination, do not touch tip of container to any surface. Replace cap after using. Stop us and ask a doctor *If condition worsens or persists for more than 72hours If pregnant or breast-feeding , ask a health professional before use Keep out of reach of children
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.