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 124 of 354 · 7,077 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Matte Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE EDIT EUROSPA, LLC 3751544d-e093-3d19-e063-6394a90aefc3 2025-12-15 Exact identifier application number: M020 Lip Crack TITANIUM DIOXIDE, ZINC OXIDE BELLAGENA SKINCARE STUDIO & SPA 37edc05c-82c3-90fe-e063-6294a90aa601 2025-12-15 Exact identifier application number: M020 Restore And Replenish ZINC OXIDE BELLAGENA SKINCARE STUDIO & SPA 37ed8525-6ae4-4e86-e063-6294a90afeb8 2025-12-15 Exact identifier application number: M020 Sunshade Daily Sun Defense TITANIUM DIOXIDE, ZINC OXIDE BELLAGENA SKINCARE STUDIO & SPA 37ee77dc-a96a-5efa-e063-6394a90affda 2025-12-15 Exact identifier application number: M020 Sunshade Mineral Sunscreen ZINC OXIDE BELLAGENA SKINCARE STUDIO & SPA 37df21f1-f36f-df43-e063-6294a90aea6f 2025-12-15 Exact identifier application number: M020 Tinted Moisturizing Mineral Sunscreen ZINC OXIDE EDIT EUROSPA, LLC 3751861d-3f3b-2ebd-e063-6294a90af898 2025-12-15 Exact identifier application number: M020 Non Tinted Moisturizing Mineral Sunscreen ZINC OXIDE EDIT EUROSPA, LLC 3751e278-b8b2-7bf4-e063-6394a90a4290 2025-12-15 Exact identifier application number: M020 Tinted Mineral Sunscreen Stick TITANIUM DIOXIDE, ZINC OXIDE EDIT EUROSPA, LLC 37521c60-2fee-861e-e063-6294a90ad69a 2025-12-15 Exact identifier application number: M020 MATTE Non Tinted Mineral Sunscreen ZINC OXIDE Allure Esthetics 3725d947-b1fa-3b50-e063-6394a90adf10 2025-12-15 Exact identifier application number: M020 GLOW Tinted Mineral Sunscreen ZINC OXIDE Allure Esthetics 37257bb2-d91d-6ff8-e063-6294a90a01b6 2025-12-15 Exact identifier application number: M020 Daily Restore ZINC OXIDE TYRLIN ENTERPRISES, INC. 35ce7133-badb-1bc4-e063-6294a90a7478 2025-12-15 Exact identifier application number: M020 20Percent Zinc Oxide Sunscreen ZINC OXIDE Minder Day Spa, Inc. 35bee5f9-68d6-6302-e063-6394a90ada88 2025-12-15 Exact identifier application number: M020 20Percent Zinc Oxide Sunscreen ZINC OXIDE Minder Day Spa, Inc. 35bfd54a-d7b7-f1a7-e063-6294a90a039b 2025-12-15 Exact identifier application number: M020 AM RESTORE ZINC OXIDE Minder Day Spa, Inc. 35c03804-04e9-3d54-e063-6294a90a3407 2025-12-15 Exact identifier application number: M020 Deflectin Tinted Mineral Sunscreen ZINC OXIDE AEON AESTHETICS LLC 35d14660-8900-2cb0-e063-6394a90a317d 2025-12-15 Exact identifier application number: M020 Mineral Tinted Lip Sunscreen TITANIUM DIOXIDE, ZINC OXIDE JADEIA LIMITED INC 35cf36c1-50c9-e848-e063-6294a90a6658 2025-12-15 Exact identifier application number: M020 Flash Invisible Stick TITANIUM DIOXIDE, ZINC OXIDE AEON AESTHETICS LLC 35d2489e-4978-4fc3-e063-6294a90adfcc 2025-12-15 Exact identifier application number: M020 AM RESTORE ZINC OXIDE Minder Day Spa, Inc. 35c010ad-e25d-f197-e063-6294a90a0efb 2025-12-15 Exact identifier application number: M020 Flash Tinted Stick TITANIUM DIOXIDE, ZINC OXIDE AEON AESTHETICS LLC 35d28590-e746-7996-e063-6294a90ac7d8 2025-12-15 Exact identifier application number: M020 Mineral Tinted Sunscreen TITANIUM DIOXIDE, ZINC OXIDE JADEIA LIMITED INC 35cf03f4-200a-5643-e063-6394a90a9e02 2025-12-15 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