Cornex

Product NDC: 56104-009
Requested package NDC: 56104-009-09
11-digit product format: 561040009
Labeler code: 56104
Product ID: 56104-009_c7045d71-6ba0-59f1-e053-2995a90a7c8d
Type: HUMAN OTC DRUG
Nonproprietary name: Corn and Callus Liquid Remover
Dosage form: LIQUID
Route: TOPICAL
Labeler: Premier Brands of America Inc.
Application: part358F
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2013-01-01
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
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	56104-009	56104-009-09	D	Discontinued by firm		2026-10-05

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 · 9 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`

Reported adverse events (FAERS/openFDA)#

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

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
SALICYLIC ACID	ACTIVE INGREDIENT	O414PZ4LPZ	CORNEX (CORN AND CALLUS LIQUID REMOVER) LIQUID [PREMIER BRANDS OF AMERICA INC.]	1
SALICYLIC ACID	ACTIVE MOIETY	O414PZ4LPZ	CORNEX (CORN AND CALLUS LIQUID REMOVER) LIQUID [PREMIER BRANDS OF AMERICA INC.]	1
CAMPHOR (NATURAL)	INACTIVE INGREDIENT	N20HL7Q941	CORNEX (CORN AND CALLUS LIQUID REMOVER) LIQUID [PREMIER BRANDS OF AMERICA INC.]	1
CASTOR OIL	INACTIVE INGREDIENT	D5340Y2I9G	CORNEX (CORN AND CALLUS LIQUID REMOVER) LIQUID [PREMIER BRANDS OF AMERICA INC.]	1
PYROXYLIN	INACTIVE INGREDIENT	KYR8BR2X6O	CORNEX (CORN AND CALLUS LIQUID REMOVER) LIQUID [PREMIER BRANDS OF AMERICA INC.]	1

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
O414PZ4LPZ	SALICYLIC ACID	69-72-7	SALICYLIC ACID

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
56104-009-09	56104000909	9 g in 1 BOTTLE, WITH APPLICATOR (56104-009-09)	9 g	2015-10-10	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Premier Brands Liquid Corn and Callus Remover	Premier Brands of America Inc.	2024-10-11	HUMAN OTC DRUG LABEL	9

Cornex

NDC auxiliary status#

Observed NDC auxiliary status history#

Reported adverse events (FAERS/openFDA)#

DailyMed Socrata Ingredients#

Related Records#

Related UNII Ingredients#

Packages#

Related DailyMed Labels#