NDC 69968-0804-01 - Clean and Clear Acne Spot Treatment

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 69968-0804
Requested NDC: 69968-0804-01
Package NDCs from labels: 69968-0804-1, 69968-0804-01
Manufacturer: Kenvue Brands LLC
Effective date: 2025-07-28
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Clean and Clear Acne Spot Treatment - Kenvue Brands LLC	Kenvue Brands LLC	2025-07-28	HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69968-0804-1	Clean and Clear Acne Spot Treatment	22 mL in 1 TUBE	GEL	22		4
69968-0804-1	Clean and Clear Acne Spot Treatment	1 in 1 CARTON	GEL	1		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69968-0804	CLEAN AND CLEAR ACNE SPOT TREATMENT (SALICYLIC ACID) GEL [KENVUE BRANDS LLC]	3	Current NDC, 2 package rows	20241114_098e0fcf-7640-e40a-e063-6394a90ac1ee.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 304 of 304 · 6,063 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
CVS Hand Sanitizer	ALCOHOL	CVS	d0081c50-c0d2-436a-ba83-5d1982ae64b7	2015-08-17	Warnings	Exact identifier unii: 3K9958V90M
Instant Hand Sanitizer	ALCOHOL	Safetec of America, Inc.	f9e30645-491b-4f54-acfd-f863ee235607	2013-08-07	Warnings	Exact identifier unii: 3K9958V90M
SKIN MEDICA Purifying Foaming Wash	SALICYLIC ACID	Allergan, Inc.	064d9e2b-077f-4229-b653-666fc5479ae2	2013-03-01	Warnings	Exact identifier application number: M006 unii: O414PZ4LPZ

Reported adverse events (FAERS/openFDA)#

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