Neutrogena Scalp Therapy Anti-Dandruff Daily Control
- Product NDC
- 69968-0722
- Requested package NDC
- 69968-0722-1
- 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
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| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69968-0722 | NEUTROGENA SCALP THERAPY ANTI-DANDRUFF DAILY CONTROL (SALICYLIC ACID) SHAMPOO [KENVUE BRANDS LLC] | 4 | Legacy NDC | 20250315_ca4944cf-7fdb-4720-e053-2995a90a35e9.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69968-0722-1 | 69968072201 | 354 mL in 1 BOTTLE, PLASTIC (69968-0722-1) | 354 ml | 2021-12-06 | 0000-00-00 | No | No | Current |