Home NDC 75124-0011 D.PRO Pack Solid
Product NDC 75124-0011
11-digit product format 751240011
Labeler code 75124
Product ID 75124-0011_c0289ea3-c593-0760-e053-2a95a90a0cfd
Type HUMAN OTC DRUG
Nonproprietary name sodium chlorite
Dosage form POWDER
Route TOPICAL
Labeler Pure O2
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2021-04-17
Substance SODIUM CHLORITE
Active strength 23 g/100g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base D.PRO Pack Solid
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 75124-0011-1 D.PRO Pack Solid 4 g in 1 CONTAINER POWDER 4 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 75124-0011 D.PRO PACK SOLID (SODIUM CHLORITE) POWDER [PURE O2] 1 Current NDC, Legacy NDC, 1 package rows 20210418_c0289ea3-c592-0760-e053-2a95a90a0cfd.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 Marketing end Sample Exclude flag Status 75124-0011-1 75124001101 4 g in 1 CONTAINER (75124-0011-1) 4 g 2021-04-17 0000-00-00 No No Current