SALZIX WART REMOVER

Product NDC
72847-333
11-digit product format
728470333
Labeler code
72847
Product ID
72847-333_b71df063-c5d7-4a4f-a638-f004158631e4
Type
HUMAN OTC DRUG
Nonproprietary name
Salicylic acid
Dosage form
LIQUID
Route
TOPICAL
Labeler
Toprail Chp Llc
Application
M028
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-03-20
Substance
SALICYLIC ACID
Active strength
.17 g/9mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
SALZIX WART REMOVER
Listing expiration
2026-12-31

Active Ingredients#

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

Harmonized Identifiers#

Field, Values table
FieldValues
UniiO414PZ4LPZ

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72847-333-29SALZIX WART REMOVER1 in 1 BOXLIQUID11
72847-333-29SALZIX WART REMOVER9 mL in 1 BOTTLE, WITH APPLICATORLIQUID91

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
72847-333-29728470333291 BOTTLE, WITH APPLICATOR in 1 BOX (72847-333-29) / 9 mL in 1 BOTTLE, WITH APPLICATOR2025-03-20NoNoCurrent