Home NDC 81488-008 Mineffect acid indigestion and heartburn relief
Product NDC 81488-008
11-digit product format 814880008
Labeler code 81488
Product ID 81488-008_09069632-9851-c1ad-e063-6294a90aa320
Type HUMAN OTC DRUG
Nonproprietary name Alumina, Calcarea Silicata, Ferrum Metallicum, Ferrum Phosphoricum, Magnesia Muriatica, Natrum Nitricum, Phosphorus, Silicea, Zincum Metallicum
Dosage form LIQUID
Route ORAL
Labeler Kadesh Incoporation Co,Ltd
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2022-01-21
Substance ALUMINUM OXIDE; CALCIUM SILICATE; FERROSOFERRIC PHOSPHATE; IRON; MAGNESIUM CHLORIDE; PHOSPHORUS; SILICON DIOXIDE; SODIUM NITRATE; ZINC
Active strength 5; 5; 7; 7; 4; 6; 4; 4; 8 [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL
Pharmacologic classes Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Mineffect acid indigestion and heartburn relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM OXIDE 5 [hp_X]/30mL CALCIUM SILICATE 5 [hp_X]/30mL IRON 7 [hp_X]/30mL FERROSOFERRIC PHOSPHATE 7 [hp_X]/30mL MAGNESIUM CHLORIDE 4 [hp_X]/30mL SODIUM NITRATE 6 [hp_X]/30mL PHOSPHORUS 4 [hp_X]/30mL SILICON DIOXIDE 4 [hp_X]/30mL ZINC 8 [hp_X]/30mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 9 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 81488-008-01 Mineffect acid indigestion and heartburn relief 1 in 1 BOX LIQUID 1 2 81488-008-01 Mineffect acid indigestion and heartburn relief 30 mL in 1 BOTTLE LIQUID 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81488-008 MINEFFECT ACID INDIGESTION AND HEARTBURN RELIEF (ALUMINA, CALCAREA SILICATA, FERRUM METALLICUM, FERRUM PHOSPHORICUM, MAGNESIA MURIATICA, NATRUM NITRICUM, PHOSPHORUS, SILICEA, ZINCUM METALLICUM) LIQUID [KADESH INCOPORATION CO,LTD] 2 Current NDC, Legacy NDC, 2 package rows 20231101_048367ff-a9bb-46a3-a835-aa3ab391eee4.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Mineffect acid indigestion and heartburn relief ALUMINA, CALCAREA SILICATA, FERRUM METALLICUM, FERRUM PHOSPHORICUM, MAGNESIA MURIATICA, NATRUM NITRICUM, PHOSPHORUS, SILICEA, ZINCUM METALLICUM Kadesh Incoporation Co,Ltd 048367ff-a9bb-46a3-a835-aa3ab391eee4 2023-10-31 Warnings Exact identifier ndc (product): 81488-008
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 81488-008-01 81488000801 1 BOTTLE in 1 BOX (81488-008-01) / 30 mL in 1 BOTTLE 1 bottle 2022-01-21 0000-00-00 No No Current