FDA.reportPublic FDA data

Neutrogena Scalp Therapy Anti-Dandruff Daily Control

Product NDC
69968-0722
11-digit product format
699680722
Labeler code
69968
Product ID
69968-0722_ef273f64-2b22-1728-e053-2995a90a85e3
Type
HUMAN OTC DRUG
Nonproprietary name
Salicylic Acid
Dosage form
SHAMPOO
Route
TOPICAL
Labeler
Johnson & Johnson Consumer Inc.
Application
part358H
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2021-12-06
Marketing end
0000-00-00
Substance
SALICYLIC ACID
Active strength
18 mg/mL
NDC exclude flag
No
Listing certified through
2024-12-31
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
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct69968-0722DDiscontinued by firm2026-10-05
excluded packagepackage69968-072269968-0722-1DDiscontinued by firm2026-10-05

Reported adverse events (FAERS/openFDA)#

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

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69968-0722NEUTROGENA SCALP THERAPY ANTI-DANDRUFF DAILY CONTROL (SALICYLIC ACID) SHAMPOO [KENVUE BRANDS LLC]4Legacy NDC20250315_ca4944cf-7fdb-4720-e053-2995a90a35e9.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69968-0722-169968072201354 mL in 1 BOTTLE, PLASTIC (69968-0722-1) 354 ml2021-12-060000-00-00NoNoCurrent