Home NDC 75124-0010 QVE - S
Product NDC 75124-0010
11-digit product format 751240010
Labeler code 75124
Product ID 75124-0010_acde31eb-b011-5f00-e053-2a95a90a36eb
Type HUMAN OTC DRUG
Nonproprietary name sodium chlorite
Dosage form POWDER
Route TOPICAL
Labeler Pure O2
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2020-08-15
Substance SODIUM CHLORITE
Active strength 23 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. Every label matching the complete exact-identifier union is deduplicated and paginated below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Additional Listing Data#
Finished product Yes
Brand name base QVE - S
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM CHLORITE 23 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination G538EBV4VF Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 75124-0010-1 QVE - S 4 g in 1 POUCH POWDER 4 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 75124-0010 QVE - S (SODIUM CHLORITE) POWDER [PURE O2] 1 Current NDC, Legacy NDC, 1 package rows 20200815_acdeca69-4e20-9502-e053-2a95a90a5327.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 75124-0010-1 75124001001 4 g in 1 POUCH (75124-0010-1) 4 g 2020-08-15 0000-00-00 No No Current