Home NDC 69968-0576 Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF55
Product NDC 69968-0576
11-digit product format 699680576
Labeler code 69968
Product ID 69968-0576_5b846de1-5c31-3f15-e063-6394a90aedd4
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Homosalate, Octisalate, and Octocrylene
Dosage form LOTION
Route TOPICAL
Labeler Kenvue Brands LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-10-07
Substance AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength 30; 100; 50; 100 mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
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 Sheer Dry Touch Sunscreen Broad Spectrum SPF55
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 30 mg/mL HOMOSALATE 100 mg/mL OCTISALATE 50 mg/mL OCTOCRYLENE 100 mg/mL
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69968-0576-1 Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF55 29 mL in 1 TUBE LOTION 29 20 69968-0576-3 Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF55 88 mL in 1 TUBE LOTION 88 20 69968-0576-5 Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF55 147 mL in 1 TUBE LOTION 147 20 69968-0576-6 Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF55 88 mL in 1 TUBE LOTION 88 20 69968-0576-6 Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF55 3 in 1 CARTON LOTION 3 20 69968-0576-3 Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF 55Clubtray 88 mL in 1 TUBE LOTION 88 mL 50 mg in 1mL 4 69968-0576-5 Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF 55Clubtray 147 mL in 1 TUBE LOTION 147 mL 30 mg in 1mL 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69968-0576 NEUTROGENA ULTRA SHEER DRY TOUCH SUNSCREEN BROAD SPECTRUM SPF55 (AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE) LOTION [KENVUE BRANDS LLC] 18 Current NDC, Legacy NDC, 5 package rows 20250308_fbd4365b-9b16-4daf-9db5-b268bd17c37a.zip 69968-0576 NEUTROGENA ULTRA SHEER DRY TOUCH SUNSCREEN BROAD SPECTRUM SPF 55 CLUBTRAY (AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE) KIT [KENVUE BRANDS LLC] 2 Current NDC, Legacy NDC 20241116_0bd538e9-7716-9bc2-e063-6294a90a9a07.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 146 of 353 · 7,049 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Safe Sea SPF 50 HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE NIDARIA TECHNOLOGY LTD 46641a33-d658-4ef0-9b7a-062adc401dde 2025-12-08 Warnings Exact identifier application number: M020 Skin Filter Glow SPF ZINC OXIDE MALORIE MILES 36485f44-a6bd-9529-e063-6294a90af7a4 2025-12-08 Exact identifier application number: M020 Skin Filter Matte SPF TITANIUM DIOXIDE, ZINC OXIDE MALORIE MILES 3647f983-9e75-8955-e063-6294a90af162 2025-12-08 Exact identifier application number: M020 Body-Screen ZINC OXIDE MALORIE MILES 36499be5-d680-92bf-e063-6394a90a89db 2025-12-08 Exact identifier application number: M020 Skin Filter Matte SPF TITANIUM DIOXIDE, ZINC OXIDE MALORIE MILES 3649f758-e31b-3c6a-e063-6294a90a5c36 2025-12-08 Exact identifier application number: M020 Body-Screen ZINC OXIDE MALORIE MILES 364ae392-480a-14ea-e063-6394a90a3883 2025-12-08 Exact identifier application number: M020 Personalized Moisturizer SPF 30 ZINC OXIDE 10.00% Proven Skincare d3cf8f81-d6ae-4570-ad86-43415e973e13 2025-12-08 Warnings Exact identifier application number: M020 GLOW SHIELD SPF ZINC OXIDE ACNE SOLUTIONS NYC INC 2f9d087c-b2b3-5654-e063-6294a90a94e5 2025-12-08 Warnings Exact identifier application number: M020 MATTE SHIELD SPF ZINC OXIDE ACNE SOLUTIONS NYC INC 2faee7ef-fc0c-6d01-e063-6294a90a6d68 2025-12-08 Warnings Exact identifier application number: M020 GLOW SHIELD SPF ZINC OXIDE ACNE SOLUTIONS NYC INC 2faf530d-5574-b702-e063-6294a90ad6fd 2025-12-08 Warnings Exact identifier application number: M020 MATTE SHIELD SPF ZINC OXIDE ACNE SOLUTIONS NYC INC 2fb00db0-4c37-56c6-e063-6294a90a8aff 2025-12-08 Warnings Exact identifier application number: M020 Matte Shield SPF TITANIUM DIOXIDE, ZINC OXIDE ACNE SOLUTIONS NYC INC 3bb582ec-71e7-4ad8-e063-6394a90a94d4 2025-12-08 Warnings Exact identifier application number: M020 SPF 101 Lightly Tinted ZINC OXIDE The Acne Lab LLC 334afdc8-1e12-d787-e063-6294a90aed7c 2025-12-08 Exact identifier application number: M020 SPF 101 Non-Tinted ZINC OXIDE The Acne Lab LLC 334bf8ea-2485-84e8-e063-6294a90aefa6 2025-12-08 Exact identifier application number: M020 SPF 101 Lightly Tinted ZINC OXIDE The Acne Lab LLC 334d694a-f9e4-ae86-e063-6394a90abfe1 2025-12-08 Exact identifier application number: M020 SPF 101 Non-Tinted ZINC OXIDE The Acne Lab LLC 334e32a4-c3a5-e37d-e063-6294a90ad6cf 2025-12-08 Exact identifier application number: M020 Mineral Based Sunscreen Stick Non-Tinted TITANIUM DIOXIDE, ZINC OXIDE KATHLEEN P. HUTTON, M.D., INC. A PROFESSIONAL CORPORATION 3245561d-a90c-7bf0-e063-6394a90ab3b6 2025-12-08 Exact identifier application number: M020 Mineral Based Sunscreen Stick Tinted TITANIUM DIOXIDE, ZINC OXIDE KATHLEEN P. HUTTON, M.D., INC. A PROFESSIONAL CORPORATION 3245c1f7-2c1b-b6ad-e063-6394a90aaee6 2025-12-08 Exact identifier application number: M020 Mineral Based Facial Sunscreen ZINC OXIDE KATHLEEN P. HUTTON, M.D., INC. A PROFESSIONAL CORPORATION 3e8981ed-5847-7009-e063-6394a90a49a1 2025-12-08 Warnings Exact identifier application number: M020 Replenishing Daily Protection Sunscreen Invisible ZINC OXIDE KATHLEEN P. HUTTON, M.D., INC. A PROFESSIONAL CORPORATION 32462e88-0e74-a675-e063-6294a90ac564 2025-12-08 Exact identifier application number: M020
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 69968-0576-1 69968057601 29 mL in 1 TUBE (69968-0576-1) 29 ml 2019-10-07 0000-00-00 No No Current 69968-0576-3 69968057603 88 mL in 1 TUBE (69968-0576-3) 88 ml 2019-10-07 0000-00-00 No No Current 69968-0576-5 69968057605 147 mL in 1 TUBE (69968-0576-5) 147 ml 2019-10-07 0000-00-00 No No Current 69968-0576-6 69968057606 3 TUBE in 1 CARTON (69968-0576-6) / 88 mL in 1 TUBE 3 tube 2019-10-07 No No Current