Home NDC 75124-0003 PURE O2STICK
Product NDC 75124-0003
11-digit product format 751240003
Labeler code 75124
Product ID 75124-0003_0a4eb0be-cd45-6702-e063-6294a90ab9a3
Type HUMAN OTC DRUG
Nonproprietary name sodium chlorite
Dosage form LIQUID
Route TOPICAL
Labeler Pure O2
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2020-04-01
Substance SODIUM CHLORITE
Active strength 5 g/100g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
warnings ■ For external use only. ■ Do not use in eyes. ■ lf swallowed, get medical help promptly. ■ Stop use, ask doctor lf irritation occurs. ■ Keep out of reach of children.
Additional Listing Data#
Finished product Yes
Brand name base PURE O2STICK
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM CHLORITE 5 g/100g
Harmonized Identifiers# Field, Values table Field Values Unii G538EBV4VF
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 75124-0003-1 PURE O2STICK 9 g in 1 PACKAGE LIQUID 9 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 75124-0003 PURE O2STICK (SODIUM CHLORITE) LIQUID [PURE O2] 4 Current NDC, Legacy NDC, 1 package rows 20231117_a39a1e99-d714-645d-e053-2995a90a024c.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 75124-0003-1 75124000301 9 g in 1 PACKAGE (75124-0003-1) 9 g 2020-04-01 0000-00-00 No No Current