Home NDC 49035-017 Maximum Strength Wart Remover with Salicylic Acid
Product NDC 49035-017
11-digit product format 490350017
Labeler code 49035
Product ID 49035-017_49dc357f-f634-5509-e063-6394a90adef2
Type HUMAN OTC DRUG
Nonproprietary name Wart Remover with Salicylic Acid
Dosage form LIQUID
Route TOPICAL
Labeler Wal-Mart Stores, Inc.
Application M028
Marketing category OTC MONOGRAPH DRUG
Marketing start 2011-12-31
Substance SALICYLIC ACID
Active strength 17 mg/100mg
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2019-12-08 06:16 UTC · source 2019-12-05 excluded product product 49035-017 E Excluded after deficient or non-compliant submission was not corrected excluded / ndc_excluded.zip 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 49035-017 49035-017-09 E Excluded after deficient or non-compliant submission was not corrected excluded / ndc_excluded.zip 110d247fa046…a55b01930146…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Maximum Strength Wart Remover with Salicylic Acid
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SALICYLIC ACID 17 mg/100mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination O414PZ4LPZ Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 312881 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 49035-017-09 Maximum Strength Wart Remover with Salicylic Acid 9000 mg in 1 BOTTLE, WITH APPLICATOR LIQUID 9000 10
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49035-017 MAXIMUM STRENGTH WART REMOVER WITH SALICYLIC ACID (WART REMOVER WITH SALICYLIC ACID) LIQUID [WAL-MART STORES, INC.] 8 Current NDC, Legacy NDC, 1 package rows 20241219_f6ab841b-9f2f-483f-89ae-9f72f391c8e6.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 16 of 16 · 305 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 49035-017-09 49035001709 9000 mg in 1 BOTTLE, WITH APPLICATOR (49035-017-09) 9000 mg 2011-12-31 0000-00-00 No No Current