Wart Remover Liquid

Product NDC: 56104-023
Requested package NDC: 56104-023-15
11-digit product format: 561040023
Labeler code: 56104
Product ID: 56104-023_d7d0361f-70d5-4fa2-959a-bfd9bbf50f94
Type: HUMAN OTC DRUG
Nonproprietary name: Wart Remover Liquid
Dosage form: LIQUID
Route: TOPICAL
Labeler: Premier Brands of America Inc.
Application: part358B
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: 2020-12-31
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	56104-023	56104-023-15	I	Inactivated by FDA		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 · 19 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…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	`1332a3947898…`	`d4bfe170f9cd…`
2022-08-30 03:57 UTC · source 2022-08-29	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	`bd6a592717d7…`	`303034d00443…`
2021-12-27 23:28 UTC · source 2021-12-27	`8dfbde2a14a4…`	`c9ff85d89658…`

Reported adverse events (FAERS/openFDA)#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277	Product name	1	20190408

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
56104-023-15	2021-07-23	C162847	48780-1	c7ccaba7-279f-fd44-e053-dadaa90aa01b	Wart Remover Liquid

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
56104-023-15	Wart Remover Liquid	15 g in 1 BOTTLE, WITH APPLICATOR	LIQUID	15		3

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
SALICYLIC ACID	ACTIVE INGREDIENT	O414PZ4LPZ	WART REMOVER LIQUID LIQUID [PREMIER BRANDS OF AMERICA INC.]	2
SALICYLIC ACID	ACTIVE MOIETY	O414PZ4LPZ	WART REMOVER LIQUID LIQUID [PREMIER BRANDS OF AMERICA INC.]	2
CAMPHOR (NATURAL)	INACTIVE INGREDIENT	N20HL7Q941	WART REMOVER LIQUID LIQUID [PREMIER BRANDS OF AMERICA INC.]	2
CASTOR OIL	INACTIVE INGREDIENT	D5340Y2I9G	WART REMOVER LIQUID LIQUID [PREMIER BRANDS OF AMERICA INC.]	2
PYROXYLIN	INACTIVE INGREDIENT	KYR8BR2X6O	WART REMOVER LIQUID LIQUID [PREMIER BRANDS OF AMERICA INC.]	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
56104-023	WART REMOVER LIQUID LIQUID [PREMIER BRANDS OF AMERICA INC.]	3	Legacy NDC, 1 package rows	20160129_1e02df48-e23e-42b2-a441-21535379de58.zip

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

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
312881	salicylic acid 17 % Topical Solution	PSN	1e02df48-e23e-42b2-a441-21535379de58	3
312881	salicylic acid 170 MG/ML Topical Solution	SCD	1e02df48-e23e-42b2-a441-21535379de58	3
312881	salicylic acid 17 % Topical Solution	SY	1e02df48-e23e-42b2-a441-21535379de58	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
56104-023-15	56104002315	15 g in 1 BOTTLE, WITH APPLICATOR (56104-023-15)	15 g	2013-01-01	0000-00-00	No	No	Current