Salicylic Acid

Product NDC
69256-035
11-digit product format
692560035
Labeler code
69256
Product ID
69256-035_40976655-12cc-fd19-e063-6394a90ad3b0
Type
HUMAN OTC DRUG
Nonproprietary name
Wart Remover Liquid
Dosage form
LIQUID
Route
TOPICAL
Labeler
Harris Teeter, LLC
Application
M028
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2017-12-21
Substance
SALICYLIC ACID
Active strength
.17 mg/9mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Salicylic Acid
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SALICYLIC ACID.17 mg/9mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiO414PZ4LPZ

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69256-035-09Salicylic Acid9 mL in 1 BOTTLE, WITH APPLICATORLIQUID98

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69256-035SALICYLIC ACID (WART REMOVER LIQUID) LIQUID [HARRIS TEETER, LLC]7Current NDC, Legacy NDC, 1 package rows20241212_d53756d4-6739-48da-b367-84531f989170.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69256-035-09692560035099 mL in 1 BOTTLE, WITH APPLICATOR (69256-035-09) 9 ml2017-12-210000-00-00NoNoCurrent