Home NDC 79988-002 Advanced Day Ultimate Protect Sunscreen SPF 50
Product NDC 79988-002
11-digit product format 799880002
Labeler code 79988
Product ID 79988-002_29071920-ba91-871a-e063-6294a90aee27
Type HUMAN OTC DRUG
Nonproprietary name Butyl Methoxydibenzoylmethane, Ethylhexyl Salicylate
Dosage form CREAM
Route TOPICAL
Labeler Medik8 Limited
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-01-06
Substance ETHYLHEXYL SALICYLATE; OCTOCRYLENE; HOMOSALATE; BUTYL METHOXYDIBENZOYLMETHANE
Active strength 4.8; 9.5; 10; 2.8 g/100mL; g/100mL; g/100mL; g/100mL
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 Advanced Day Ultimate Protect Sunscreen SPF 50
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ETHYLHEXYL SALICYLATE 4.8 g/100mL OCTOCRYLENE 9.5 g/100mL HOMOSALATE 10 g/100mL BUTYL METHOXYDIBENZOYLMETHANE 2.8 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 79988-002-05 Advanced Day Ultimate Protect Sunscreen SPF 50 5 mL in 1 BOTTLE CREAM 5 1 79988-002-50 Advanced Day Ultimate Protect Sunscreen SPF 50 50 mL in 1 BOTTLE CREAM 50 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 79988-002 ADVANCED DAY ULTIMATE PROTECT SUNSCREEN SPF 50 (BUTYL METHOXYDIBENZOYLMETHANE, ETHYLHEXYL SALICYLATE) CREAM [MEDIK8 LIMITED] 1 Current NDC, 2 package rows 20250109_29071920-ba90-871a-e063-6294a90aee27.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 148 of 353 · 7,049 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Mineral SPF 40, Tinted TITANIUM DIOXIDE, ZINC OXIDE Acne Specialists LLC 2fb14c4f-a435-aa6e-e063-6394a90a7d8d 2025-12-08 Warnings Exact identifier application number: M020 Mineral Sunscreen SPF 40 Non-Tinted TITANIUM DIOXIDE, ZINC OXIDE Skin Restoration Aesthetics 2fc4f701-eea2-7913-e063-6294a90a8693 2025-12-08 Warnings Exact identifier application number: M020 Mineral Sunscreen SPF 40 Tinted TITANIUM DIOXIDE, ZINC OXIDE Skin Restoration Aesthetics 2fc55e8c-41d6-15cc-e063-6394a90ac543 2025-12-08 Warnings Exact identifier application number: M020 Zinc Oxide SPF 40 Tinted ZINC OXIDE Skin Restoration Aesthetics 2fc60a39-789b-3d11-e063-6294a90a9abf 2025-12-08 Warnings Exact identifier application number: M020 Zinc Oxide SPF 40 Non-Tinted ZINC OXIDE Skin Restoration Aesthetics 2fc68041-acfe-8db6-e063-6294a90ad8ba 2025-12-08 Warnings Exact identifier application number: M020 Daily Tinted Mineral SPF TITANIUM DIOXIDE, ZINC OXIDE Skin Restoration Aesthetics 2fc6e168-b2c1-bf9d-e063-6394a90aade7 2025-12-08 Warnings Exact identifier application number: M020 Ultra Solar Shield non-tinted moisturizing mineral SPF 40 ZINC OXIDE Joyce Kelly Enterprises 365bdf7a-c034-beef-e063-6394a90a4dd7 2025-12-08 Exact identifier application number: M020 UV Shade tinted matte mineral SPF 40 TITANIUM DIOXIDE, ZINC OXIDE Joyce Kelly Enterprises 365b3a1e-8410-da06-e063-6294a90a462f 2025-12-08 Exact identifier application number: M020 Solar Shield non-tinted matte mineral SPF 40 TITANIUM DIOXIDE, ZINC OXIDE Joyce Kelly Enterprises 365b68a0-0f89-0f43-e063-6294a90a5eee 2025-12-08 Exact identifier application number: M020 Ultra UV Shade tinted moisturizing mineral SPF 40 ZINC OXIDE Joyce Kelly Enterprises 365ba78a-b7df-a31f-e063-6394a90a1673 2025-12-08 Exact identifier application number: M020 Mineral Sunscreen tinted TITANIUM DIOXIDE, ZINC OXIDE Face 5, LLC 3000a0a7-2b51-b832-e063-6294a90a4a08 2025-12-08 Warnings Exact identifier application number: M020 Non-Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE Face 5, LLC 3001028b-bb36-04ec-e063-6294a90a1e49 2025-12-08 Warnings Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE Face 5, LLC 3001aa3a-cc8b-6ad4-e063-6394a90a223f 2025-12-08 Warnings Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE Face 5, LLC 300268ff-f9ef-1006-e063-6294a90a5fdf 2025-12-08 Warnings Exact identifier application number: M020 Illuminating Daily SPF 40 Lightly Tinted ZINC OXIDE Face 5, LLC 3001ef4f-4cbb-8931-e063-6394a90a5cef 2025-12-08 Warnings Exact identifier application number: M020 Illuminating Daily SPF40 Non-Tinted ZINC OXIDE Face 5, LLC 300218c9-65cf-d984-e063-6294a90a1517 2025-12-08 Warnings Exact identifier application number: M020 Illuminating Daily SPF 40 Lightly Tinted ZINC OXIDE Face 5, LLC 300303e7-ef89-7449-e063-6294a90ac811 2025-12-08 Warnings Exact identifier application number: M020 Clear Path Tinted Facial Sunscreen TITANIUM DIOXIDE, ZINC OXIDE LULUS SPA BOUTIQUE 37657755-fa82-88a0-e063-6394a90ade47 2025-12-08 Exact identifier application number: M020 Tinted Lip Sunscreen TITANIUM DIOXIDE, ZINC OXIDE Dermacare 376468ce-8d9b-b672-e063-6294a90a0bd1 2025-12-08 Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE Dermacare 37643884-f186-fb54-e063-6394a90a450f 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 Sample Exclude flag Status 79988-002-05 79988000205 5 mL in 1 BOTTLE (79988-002-05) 5 ml 2025-01-06 No No Current 79988-002-50 79988000250 50 mL in 1 BOTTLE (79988-002-50) 50 ml 2025-01-06 No No Current