Home NDC 81488-012 MEB Puri-Mega
Product NDC 81488-012
11-digit product format 814880012
Labeler code 81488
Product ID 81488-012_018125f2-ad4c-b38a-e063-6294a90a7f6e
Type HUMAN OTC DRUG
Nonproprietary name MEB Puri-Mega
Dosage form LIQUID
Route ORAL
Labeler Kadesh Incoporation Co,Ltd
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2023-08-18
Substance TITANIUM; SODIUM NITRATE; FERROSOFERRIC PHOSPHATE; CALCIUM FLUORIDE; MAGNESIUM SULFATE HEPTAHYDRATE; SULFUR; MAGNESIUM CHLORIDE; SILICON DIOXIDE; PHOSPHORUS; ZINC; FERRIC CHLORIDE HEXAHYDRATE
Active strength 7; 5; 7; 6; 7; 4; 7; 4; 6; 8; 7 [hp_X]/300mL; [hp_X]/300mL; [hp_X]/300mL; [hp_X]/300mL; [hp_X]/300mL; [hp_X]/300mL; [hp_X]/300mL; [hp_X]/300mL; [hp_X]/300mL; [hp_X]/300mL; [hp_X]/300mL
Pharmacologic classes Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Iron [CS], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Parenteral Iron Replacement [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 Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base MEB Puri-Mega
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM 7 [hp_X]/300mL SODIUM NITRATE 5 [hp_X]/300mL FERROSOFERRIC PHOSPHATE 7 [hp_X]/300mL CALCIUM FLUORIDE 6 [hp_X]/300mL MAGNESIUM SULFATE HEPTAHYDRATE 7 [hp_X]/300mL SULFUR 4 [hp_X]/300mL MAGNESIUM CHLORIDE 7 [hp_X]/300mL SILICON DIOXIDE 4 [hp_X]/300mL PHOSPHORUS 6 [hp_X]/300mL ZINC 8 [hp_X]/300mL FERRIC CHLORIDE HEXAHYDRATE 7 [hp_X]/300mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 11 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 81488-012-03 MEB Puri-Mega 300 mL in 1 BOTTLE LIQUID 300 1 81488-012-10 MEB Puri-Mega 1000 mL in 1 BOTTLE LIQUID 1000 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81488-012 MEB PURI-MEGA LIQUID [KADESH INCOPORATION CO,LTD] 1 Current NDC, 2 package rows 20230822_018125f2-ad4b-b38a-e063-6294a90a7f6e.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 81488-012-03 81488001203 300 mL in 1 BOTTLE (81488-012-03) 300 ml 2023-08-18 No No Current 81488-012-10 81488001210 1000 mL in 1 BOTTLE (81488-012-10) 1000 ml 2023-08-18 No No Current