Perfect Purity Medicated Foot Powder

Product NDC
42669-201
Requested package NDC
42669-201-01
11-digit product format
426690201
Labeler code
42669
Product ID
42669-201_ef17805e-080e-0c49-e053-2a95a90a16b6
Type
HUMAN OTC DRUG
Nonproprietary name
menthol
Dosage form
POWDER
Route
TOPICAL
Labeler
Davion, Inc.
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2010-10-15
Marketing end
0000-00-00
Substance
MENTHOL
Active strength
1 g/100g
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage42669-20142669-201-01DDiscontinued by firm2026-07-31

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
42669-201-012022-12-05C16284748780-19d75b9d0-92c5-f424-e053-dadaa90a57cePerfect Purity Medicated Foot Powder
42669-201-012020-01-31C16284748780-19d75b9d0-92c5-f424-e053-dadaa90a57cePerfect Purity Medicated Foot Powder

DailyMed Socrata Ingredients#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
42669-201-0142669020101283 g in 1 CONTAINER (42669-201-01) 283 g2022-12-050000-00-00NoNoCurrent