United States · FDA National Drug Code directory

MEB Puri-Mega

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
81488-012_018125f2-ad4c-b38a-e063-6294a90a7f6e
Product NDC
81488-012
Form
LIQUID
Composition / generic term
MEB Puri-Mega
Labeler
Kadesh Incoporation Co,Ltd
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
20230818
Source listing expiry
20261231

Source-listed ingredients

  • 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

These values do not establish equivalence or a dose recommendation.

Packages

  • 300 mL in 1 BOTTLE (81488-012-03) · 81488-012-03
  • 1000 mL in 1 BOTTLE (81488-012-10) · 81488-012-10

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →