Home NDC 69968-0654-01 NDC 69968-0654-01 - Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF 70 This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 69968-0654
Requested NDC 69968-0654-01
Package NDCs from labels 69968-0654-5, 69968-0654-3, 69968-0654-1, 69968-0654-6, 69968-0654-2, 69968-0654-01
Manufacturer Kenvue Brands LLC
Effective date 2025-10-17
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69968-0654-1 Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF 70 12 in 1 CARTON LOTION 12 14 69968-0654-1 Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF 70 14 mL in 1 TUBE LOTION 14 14 69968-0654-2 Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF 70 29 mL in 1 TUBE LOTION 29 14 69968-0654-3 Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF 70 88 mL in 1 TUBE LOTION 88 14 69968-0654-5 Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF 70 147 mL in 1 TUBE LOTION 147 14 69968-0654-6 Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF 70 88 mL in 1 TUBE LOTION 88 14 69968-0654-6 Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF 70 3 in 1 CARTON LOTION 3 14
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69968-0654 NEUTROGENA ULTRA SHEER DRY TOUCH SUNSCREEN BROAD SPECTRUM SPF 70 (AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE) LOTION [KENVUE BRANDS LLC] 12 Current NDC, Legacy NDC, 7 package rows 20250215_c5a67314-e5b2-4dd6-94e9-39c2f286c346.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 145 of 428 · 8,560 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Proper Protection Plus Primer Tinted TITANIUM DIOXIDE, ZINC OXIDE Skin & Proper LLC 359723bb-6152-9566-e063-6294a90a59e0 2025-12-15 Exact identifier application number: M020 Daily Skin Protection Sunscreen Tinted ZINC OXIDE SKINPLUSBYOROYO LLC 35aa194a-9a2e-2b5f-e063-6294a90a9877 2025-12-15 Exact identifier application number: M020 Proper Protection Plus Primer NT TITANIUM DIOXIDE, ZINC OXIDE Skin & Proper LLC 3596cd73-0811-32bc-e063-6394a90ad132 2025-12-15 Exact identifier application number: M020 Proper Protection Plus Primer Tinted TITANIUM DIOXIDE, ZINC OXIDE Skin & Proper LLC 359782d7-6601-7d96-e063-6394a90af9dc 2025-12-15 Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE ESTHETICS BY RIKI LLC 37f1b692-0b80-0536-e063-6294a90ae863 2025-12-15 Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE ESTHETICS BY RIKI LLC 387d5194-bc12-68c1-e063-6394a90ab152 2025-12-15 Exact identifier application number: M020 Tinted Mineral Sun Protectant TITANIUM DIOXIDE, ZINC OXIDE PANDA PAMPERING LLC 387c23c2-a9f0-f484-e063-6394a90a4104 2025-12-15 Exact identifier application number: M020 Tinted Mineral Sun Protectant TITANIUM DIOXIDE, ZINC OXIDE PANDA PAMPERING LLC 387be96f-8cda-ce02-e063-6394a90abea5 2025-12-15 Exact identifier application number: M020 Serum Lightly Tinted ZINC OXIDE PANDA PAMPERING LLC 387c593b-c65b-62b5-e063-6294a90ac4c2 2025-12-15 Exact identifier application number: M020 Serum Lightly Tinted ZINC OXIDE PANDA PAMPERING LLC 387c9167-638c-1e30-e063-6394a90a9374 2025-12-15 Exact identifier application number: M020 REJUVN8 TITANIUM DIOXIDE, ZINC OXIDE FLEUR DE VIE LLC 37ede476-43b6-a7c8-e063-6294a90a3e8f 2025-12-15 Exact identifier application number: M020 REJUVN8 TITANIUM DIOXIDE, ZINC OXIDE FLEUR DE VIE LLC 37efa5e1-e88e-d251-e063-6394a90a9371 2025-12-15 Exact identifier application number: M020 Non-Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE THE BEAUTY ROOM OC INC 3dd330bf-92e4-3664-e063-6294a90a0475 2025-12-15 Warnings Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE THE BEAUTY ROOM OC INC 3dd37dd1-fd43-7af4-e063-6394a90ae3a0 2025-12-15 Warnings Exact identifier application number: M020 Non-Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE THE BEAUTY ROOM OC INC 3dd3dcab-e9fb-0ef5-e063-6394a90acef1 2025-12-15 Warnings Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE THE BEAUTY ROOM OC INC 3dd40a6a-d52e-ab87-e063-6294a90a966e 2025-12-15 Warnings Exact identifier application number: M020 20 Zinc Oxide Non-Tinted Mineral Sunscreen ZINC OXIDE AGELESS SKINCARE INC 3766e6c0-8976-509d-e063-6394a90af00f 2025-12-15 Exact identifier application number: M020 20 Zinc Oxide Tinted Mineral Sunscreen ZINC OXIDE AGELESS SKINCARE INC 3766b00f-ceda-a6f9-e063-6294a90aff5d 2025-12-15 Exact identifier application number: M020 Mattifying Skin Primer TITANIUM DIOXIDE, ZINC OXIDE SKIN MAVEN 37662032-2842-1982-e063-6294a90a49a0 2025-12-15 Exact identifier application number: M020 Moisturizing Face and Body SPF ZINC OXIDE SKIN MAVEN 376645ee-7ea8-e738-e063-6394a90a119b 2025-12-15 Exact identifier application number: M020
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.