Home FDA labels 09069632-9851-c1ad-e063-6294a90aa320 Mineffect acid indigestion and heartburn 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 acid indigestion and heartburn relief
Generic name ALUMINA, CALCAREA SILICATA, FERRUM METALLICUM, FERRUM PHOSPHORICUM, MAGNESIA MURIATICA, NATRUM NITRICUM, PHOSPHORUS, SILICEA, ZINCUM METALLICUM
Manufacturer Kadesh Incoporation Co,Ltd
Product type HUMAN OTC DRUG
SPL set ID 048367ff-a9bb-46a3-a835-aa3ab391eee4
SPL ID 09069632-9851-c1ad-e063-6294a90aa320
Version 2
Effective date 2023-10-31
Source export date 2026-10-12
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/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 01:32:31 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 · 17 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Mineffect acid indigestion and heartburn relief openfda.brand_name generic name ALUMINA, CALCAREA SILICATA, FERRUM METALLICUM, FERRUM PHOSPHORICUM, MAGNESIA MURIATICA, NATRUM NITRICUM, PHOSPHORUS, SILICEA, ZINCUM METALLICUM openfda.generic_name manufacturer name Kadesh Incoporation Co,Ltd openfda.manufacturer_name ndc package 81488-008-01 openfda.package_ndc ndc product 81488-008 openfda.product_ndc ndc11 package 81488000801 derived:openfda.package_ndc spl id 09069632-9851-c1ad-e063-6294a90aa320 id spl set id 048367ff-a9bb-46a3-a835-aa3ab391eee4 set_id unii 27YLU75U4W openfda.unii unii 02F3473H9O openfda.unii unii LMI26O6933 openfda.unii unii ETJ7Z6XBU4 openfda.unii unii 91GQH8I5F7 openfda.unii unii 8M4L3H2ZVZ openfda.unii unii E1UOL152H7 openfda.unii unii S4255P4G5M openfda.unii unii J41CSQ7QDS 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 Warning Do not Use *If the tamper resistant label is broken. Consult a physician if: • Symptoms persist for more than 7 days or worsen. • Inflammation, fever, or infection develops. When using this produc t *To avoid contamination, do not touch tip of container to any surface. Replace cap after using. 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.