PURISTIC

Product NDC
76648-0001
11-digit product format
766480001
Labeler code
76648
Product ID
76648-0001_a41dd403-f62c-6538-e053-2995a90a0be5
Type
HUMAN OTC DRUG
Nonproprietary name
SODIUM CHLORITE
Dosage form
LIQUID
Route
TOPICAL
Labeler
Purgofarm Co Ltd
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2020-04-10
Marketing end
0000-00-00
Substance
SODIUM CHLORITE
Active strength
5 g/100mL
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76648-0001-12023-01-30C16284748780-1f386c649-c134-0266-e053-dadaa90a7c1aCT Cosmetics Co., Ltd - Hug Lets CC Hand Sanitizer Gel(Ethanol)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76648-0001-1PURISTIC6 mL in 1 SYRINGE, PLASTICLIQUID61

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76648-0001PURISTIC (SODIUM CHLORITE) LIQUID [PURGOFARM CO LTD]1Legacy NDC, 1 package rows20200426_a41dd3c6-31cf-c49c-e053-2a95a90aec50.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
76648-0001-1766480001016 mL in 1 SYRINGE, PLASTIC (76648-0001-1) 6 ml2020-04-100000-00-00NoNoCurrent