Home NDC 69968-0890-2 Neutrogena Ultra Gentle Daily Facial Moisturizer Sunscreen Broad Spectrum SPF 30
Product NDC 69968-0890
Requested package NDC 69968-0890-2
11-digit product format 699680890
Labeler code 69968
Product ID 69968-0890_5cc68ba8-ba4c-59d0-e063-6294a90a9651
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Homosalate, Octisalate, Octocrylene
Dosage form LOTION
Route TOPICAL
Labeler Kenvue Brands LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-06-06
Substance HOMOSALATE; OCTOCRYLENE; OCTISALATE; AVOBENZONE
Active strength 80; 80; 50; 25 mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Neutrogena Ultra Gentle Daily Facial Moisturizer Sunscreen Broad Spectrum SPF 30
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 80 mg/mL OCTOCRYLENE 80 mg/mL OCTISALATE 50 mg/mL AVOBENZONE 25 mg/mL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69968-0890-1 Neutrogena Ultra Gentle Daily Facial Moisturizer Sunscreen Broad Spectrum SPF 30 1 mL in 1 POUCH LOTION 1 5 69968-0890-2 Neutrogena Ultra Gentle Daily Facial Moisturizer Sunscreen Broad Spectrum SPF 30 24 in 1 TRAY LOTION 24 5 69968-0890-2 Neutrogena Ultra Gentle Daily Facial Moisturizer Sunscreen Broad Spectrum SPF 30 1.4 mL in 1 POUCH LOTION 1.4 5 69968-0890-3 Neutrogena Ultra Gentle Daily Facial Moisturizer Sunscreen Broad Spectrum SPF 30 100 mL in 1 TUBE LOTION 100 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69968-0890 NEUTROGENA ULTRA GENTLE DAILY FACIAL MOISTURIZER SUNSCREEN BROAD SPECTRUM SPF 30 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [KENVUE BRANDS LLC] 4 Current NDC, 4 package rows 20241105_1659f2ac-5dbc-553e-e063-6394a90a9a4d.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 45 of 354 · 7,077 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 69968-0890-2 69968089002 24 POUCH in 1 TRAY (69968-0890-2) / 1.4 mL in 1 POUCH 24 pouch 2024-06-06 No No Current