Salicate

Product NDC
59088-214
11-digit product format
590880214
Labeler code
59088
Product ID
59088-214_fd699cfb-8ca0-ebb8-e053-6394a90ace4a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Salicylic Acid 10%
Dosage form
GEL
Route
TOPICAL
Labeler
PureTek Coproration
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2023-10-13
Substance
SALICYLIC ACID
Active strength
10 mg/100mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SALICYLIC ACID10 mg/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiO414PZ4LPZ

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59088-214-03Salicate30 mL in 1 BOTTLE, DROPPERGEL301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59088-214SALICATE (SALICYLIC ACID 10%) GEL [PURETEK COPRORATION]1Current NDC, 1 package rows20231014_fd699cfb-8c9f-ebb8-e053-6394a90ace4a.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
59088-214-035908802140330 mL in 1 BOTTLE, DROPPER (59088-214-03) 30 ml2023-10-13NoNoHistorical