United States · FDA National Drug Code directory

DEFENDER SIGNATURE

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
75124-0012_c0293cb2-be63-25bb-e053-2995a90a9d6a
Product NDC
75124-0012
Form
POWDER
Composition / generic term
sodium chlorite
Labeler
Pure O2
Marketing category
UNAPPROVED DRUG OTHER
Marketing start / end (source format)
20210417
Source listing expiry
20261231

Source-listed ingredients

  • SODIUM CHLORITE — 23 g/100g

These values do not establish equivalence or a dose recommendation.

Packages

  • 4 g in 1 CONTAINER (75124-0012-1) · 75124-0012-1

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.

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