SALICYLIC ACID

Product NDC: 73352-107
11-digit product format: 733520107
Labeler code: 73352
Product ID: 73352-107_f3624842-c107-40f2-b7e0-2cb82c681cf1
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: SALICYLIC ACID
Dosage form: OINTMENT
Route: TOPICAL
Labeler: Trifluent Pharma, LLC
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2022-02-15
Marketing end: 0000-00-00
Substance: SALICYLIC ACID
Active strength: 30 mg/g
NDC exclude flag: No
Listing certified through: 2023-12-31
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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	73352-107		D	Discontinued by firm		2026-10-05
excluded package	package	73352-107	73352-107-30	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 · 4 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	73352-107-30	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	73352-107-30	`f5e01cc5f278…`	`a2eaf40c39c3…`

Reported adverse events (FAERS/openFDA)#

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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
73352-107-30	GM - Gram	73352-107	35cc0157-bdb6-4cab-b916-63f03d46e69a	1	2022-08-04

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73352-107	SALICYLIC ACID OINTMENT [TRIFLUENT PHARMA LLC]	4	Legacy NDC	20240112_27c9095e-7d3b-46b0-bf34-e34bf815f77d.zip

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
73352-107-30	73352010730	1 TUBE in 1 CARTON (73352-107-30) > 30 g in 1 TUBE	1 tube	2022-02-15	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Salicyclic Acid 3% with Benzoic Acid and Oak Bark Extract	Trifluent Pharma LLC \| Dynamic Pharmaceuticals	2024-01-10	HUMAN PRESCRIPTION DRUG LABEL	4