TULA acne clearing and tone correcting gel

Product NDC: 72296-010
Requested package NDC: 72296-010-30
11-digit product format: 722960010
Labeler code: 72296
Product ID: 72296-010_d8df491f-d0ec-43f8-b401-b7e051f5005c
Type: HUMAN OTC DRUG
Nonproprietary name: TULA acne clearing and tone correcting gel
Dosage form: LIQUID
Route: TOPICAL
Labeler: Tula Life LLC
Application: part333D
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2022-12-26
Marketing end: 0000-00-00
Substance: SALICYLIC ACID
Active strength: 2 g/100g
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 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	72296-010	72296-010-30	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, Code, Status table
Captured / source date	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	D	Discontinued by firm	`f5e01cc5f278…`	`a2eaf40c39c3…`
2020-12-18 03:04 UTC · source 2020-12-17	I	Inactivated by FDA	`e2bbac7714bc…`	`27bdfed8d636…`
2020-06-10 20:45 UTC · source 2020-06-10	I	Inactivated by FDA	`9bebd1f3094a…`	`5416666fcb17…`

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
NDC	Effective	Action	Document	Indexing SPL	Related label
72296-010-30	2021-12-14	C162847	48780-1	9d75b9d1-1317-f424-e053-dadaa90a57ce	TULA acne clearing and tone correcting gel
72296-010-30	2020-01-31	C162847	48780-1	9d75b9d1-1317-f424-e053-dadaa90a57ce	TULA acne clearing and tone correcting gel

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72296-010	TULA ACNE CLEARING AND TONE CORRECTING GEL LIQUID [TULA LIFE LLC]	4	Legacy NDC	20241211_fe742404-9a2f-433c-bcf8-904231c16400.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
72296-010-30	72296001030	1 TUBE in 1 CARTON (72296-010-30) > 30 g in 1 TUBE	1 tube	2022-12-26	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
TULA acne clearing and tone correcting gel	Tula Life LLC	2024-12-06	HUMAN OTC DRUG LABEL	4
TULA Skincare Clear Skin Starters Travel-size Acne and Blemish Fighting Kit	TULA Life LLC \| Paragon Packaging Inc	2024-12-06	HUMAN OTC DRUG LABEL	3