Callus Removal Foot Pack

Product NDC
69264-016
11-digit product format
692640016
Labeler code
69264
Product ID
69264-016_eee53321-ca57-416f-8c1e-36f205a387a7
Type
HUMAN OTC DRUG
Nonproprietary name
Salicylic acid
Dosage form
PATCH
Route
TOPICAL
Labeler
POLAROISIN INTERNATIONAL CO., LTD.
Application
part358F
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2015-12-17
Marketing end
0000-00-00
Substance
SALICYLIC ACID
Active strength
12 mg/21
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69264-016-252020-01-31C16284748780-19d75b9d1-0486-f424-e053-dadaa90a57ceCallus Removal Foot Pack

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69264-016-25Callus Removal Foot Pack2 in 1 BAGPATCH21

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69264-016CALLUS REMOVAL FOOT PACK (SALICYLIC ACID) PATCH [POLAROISIN INTERNATIONAL CO., LTD.]1Legacy NDC, 1 package rows20160111_883d2910-084b-4a80-b30e-e7bdff8087ce.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
69264-016-25692640016252 in 1 BAGHistorical