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

Additional Listing Data#

Finished product
Yes
Brand name base
PURE O2STICK
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SODIUM CHLORITE5 g/100g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiG538EBV4VF

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75124-0003-12023-11-14C16284748780-1f386c64a-0b8f-0266-e053-dadaa90a7c1aDrug Facts
75124-0003-12023-01-30C16284748780-1f386c64a-0b8f-0266-e053-dadaa90a7c1aDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75124-0003-1PURE O2STICK9 g in 1 PACKAGELIQUID94

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75124-0003PURE O2STICK (SODIUM CHLORITE) LIQUID [PURE O2]4Current NDC, Legacy NDC, 1 package rows20231117_a39a1e99-d714-645d-e053-2995a90a024c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
75124-0003-1751240003019 g in 1 PACKAGE (75124-0003-1) 9 g2020-04-010000-00-00NoNoCurrent