FDA.reportPublic FDA data

Salicylic Acid

Product NDC
49035-018
Requested package NDC
49035-018-09
11-digit product format
490350018
Labeler code
49035
Product ID
49035-018_c6f1b414-4338-73b5-e053-2a95a90a683e
Type
HUMAN OTC DRUG
Nonproprietary name
Liquid Corn and Callus Remover
Dosage form
LIQUID
Route
TOPICAL
Labeler
Wal-Mart Stores, Inc.
Application
part358F
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2014-03-04
Marketing end
0000-00-00
Substance
SALICYLIC ACID
Active strength
0 g/g
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage49035-01849035-018-09DDiscontinued by firm2026-10-05

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49035-018-092023-01-31C16284748780-1f386c649-d1f5-0266-e053-dadaa90a7c1aEquate Liquid Corn & Callus Remover
49035-018-092023-01-30C16284748780-1f386c649-d1f5-0266-e053-dadaa90a7c1aEquate Liquid Corn & Callus Remover

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49035-018-09Salicylic Acid9 g in 1 BOTTLE, WITH APPLICATORLIQUID910

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
49035-018-09EA - Each49035-018d8834b7b-fbca-4c55-9462-015cff02b03a12024-04-05

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SALICYLIC ACIDACTIVE INGREDIENTO414PZ4LPZSALICYLIC ACID (LIQUID CORN AND CALLUS REMOVER) LIQUID [WAL-MART STORES, INC.]1
SALICYLIC ACIDACTIVE MOIETYO414PZ4LPZSALICYLIC ACID (LIQUID CORN AND CALLUS REMOVER) LIQUID [WAL-MART STORES, INC.]1
CAMPHOR (NATURAL)INACTIVE INGREDIENTN20HL7Q941SALICYLIC ACID (LIQUID CORN AND CALLUS REMOVER) LIQUID [WAL-MART STORES, INC.]1
CASTOR OILINACTIVE INGREDIENTD5340Y2I9GSALICYLIC ACID (LIQUID CORN AND CALLUS REMOVER) LIQUID [WAL-MART STORES, INC.]1
PYROXYLININACTIVE INGREDIENTKYR8BR2X6OSALICYLIC ACID (LIQUID CORN AND CALLUS REMOVER) LIQUID [WAL-MART STORES, INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49035-018SALICYLIC ACID (LIQUID CORN AND CALLUS REMOVER) LIQUID [WAL-MART STORES, INC.]9Legacy NDC, 1 package rows20241219_b68e81a3-51c8-4dcb-9cb7-8d8d22983b81.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
312881salicylic acid 17 % Topical SolutionPSNb68e81a3-51c8-4dcb-9cb7-8d8d22983b8110
312881salicylic acid 170 MG/ML Topical SolutionSCDb68e81a3-51c8-4dcb-9cb7-8d8d22983b8110
312881salicylic acid 17 % Topical SolutionSYb68e81a3-51c8-4dcb-9cb7-8d8d22983b8110

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
49035-018-09490350018099 g in 1 BOTTLE, WITH APPLICATOR (49035-018-09) 9 g2014-03-040000-00-00NoNoCurrent