Home NDC 69968-0776 Neutrogena Mineral Ultra Sheer Dry Touch SPF 30
Product NDC 69968-0776
11-digit product format 699680776
Labeler code 69968
Product ID 69968-0776_2e05bab2-d985-745f-e063-6294a90a7892
Type HUMAN OTC DRUG
Nonproprietary name Titanium Dioxide, Zinc Oxide
Dosage form LOTION
Route TOPICAL
Labeler Kenvue Brands LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-12-06
Substance ZINC OXIDE; TITANIUM DIOXIDE
Active strength 180; 66 mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
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 Mineral Ultra Sheer Dry Touch SPF 30
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 180 mg/mL TITANIUM DIOXIDE 66 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup 15FIX9V2JP Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69968-0776-1 Neutrogena Mineral Ultra Sheer Dry Touch SPF 30 14 mL in 1 TUBE LOTION 14 5 69968-0776-1 Neutrogena Mineral Ultra Sheer Dry Touch SPF 30 12 in 1 TRAY LOTION 12 5 69968-0776-2 Neutrogena Mineral Ultra Sheer Dry Touch SPF 30 88 mL in 1 TUBE LOTION 88 5 69968-0776-2 Neutrogena Mineral Ultra Sheer Dry Touch SPF 30 2 in 1 TRAY LOTION 2 5 69968-0776-3 Neutrogena Mineral Ultra Sheer Dry Touch SPF 30 88 mL in 1 TUBE LOTION 88 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69968-0776 NEUTROGENA MINERAL ULTRA SHEER DRY TOUCH SPF 30 (TITANIUM DIOXIDE, ZINC OXIDE) LOTION [KENVUE BRANDS LLC] 5 Current NDC, Legacy NDC, 5 package rows 20250215_e99311c2-ed8b-6e60-e053-2a95a90a9bc2.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 26 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 69968-0776-1 69968077601 12 TUBE in 1 TRAY (69968-0776-1) / 14 mL in 1 TUBE 12 tube 2022-12-06 0000-00-00 No No Current 69968-0776-2 69968077602 2 TUBE in 1 TRAY (69968-0776-2) / 88 mL in 1 TUBE 2 tube 2024-02-01 No No Current 69968-0776-3 69968077603 88 mL in 1 TUBE (69968-0776-3) 88 ml 2022-12-06 0000-00-00 No No Current