Salicylic Acid

Product NDC
68016-632
11-digit product format
680160632
Labeler code
68016
Product ID
68016-632_c78ddd70-f29a-b5c3-e053-2995a90ae1ff
Type
HUMAN OTC DRUG
Nonproprietary name
Wart Remover Gel
Dosage form
GEL
Route
TOPICAL
Labeler
Chain Drug Consortium, LLC
Application
part358B
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2011-10-20
Marketing end
0000-00-00
Substance
SALICYLIC ACID
Active strength
0 g/7g
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68016-632SALICYLIC ACID (WART REMOVER GEL) GEL [CHAIN DRUG CONSORTIUM, LLC]9Legacy NDC20241213_c8dd473b-9683-471f-b60d-349f12b1c1e1.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68016-632-00680160632007 g in 1 TUBE (68016-632-00) 7 g2011-10-200000-00-00NoNoCurrent