advanced day ultimate protect sunscreen spf 50

Generic: butyl methoxydibenzoylmethane, ethylhexyl salicylate

Labeler: medik8 limited
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name advanced day ultimate protect sunscreen spf 50
Generic Name butyl methoxydibenzoylmethane, ethylhexyl salicylate
Labeler medik8 limited
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

butyl methoxydibenzoylmethane 2.8 g/100mL, ethylhexyl salicylate 4.8 g/100mL, homosalate 10 g/100mL, octocrylene 9.5 g/100mL

Manufacturer
Medik8 Limited

Identifiers & Regulatory

Product NDC 79988-002
Product ID 79988-002_29071920-ba91-871a-e063-6294a90aee27
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2025-01-06

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 79988002
Hyphenated Format 79988-002

Supplemental Identifiers

UPC
0818625027254
UNII
G63QQF2NOX 4X49Y0596W V06SV4M95S 5A68WGF6WM

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name advanced day ultimate protect sunscreen spf 50 (source: ndc)
Generic Name butyl methoxydibenzoylmethane, ethylhexyl salicylate (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 2.8 g/100mL
  • 4.8 g/100mL
  • 10 g/100mL
  • 9.5 g/100mL
source: ndc
Packaging
  • 5 mL in 1 BOTTLE (79988-002-05)
  • 50 mL in 1 BOTTLE (79988-002-50)
source: ndc

Packages (2)

79988-002-05 5 mL in 1 BOTTLE (79988-002-05) 79988-002-50 50 mL in 1 BOTTLE (79988-002-50)

Ingredients (4)

butyl methoxydibenzoylmethane (2.8 g/100mL) ethylhexyl salicylate (4.8 g/100mL) homosalate (10 g/100mL) octocrylene (9.5 g/100mL)

Linked Drug Pages (1)

Advanced Day Ultimate Protect Sunscreen SPF 50 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "29071920-ba91-871a-e063-6294a90aee27", "openfda": {"upc": ["0818625027254"], "unii": ["G63QQF2NOX", "4X49Y0596W", "V06SV4M95S", "5A68WGF6WM"], "spl_set_id": ["29071920-ba90-871a-e063-6294a90aee27"], "manufacturer_name": ["Medik8 Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 BOTTLE (79988-002-05)", "package_ndc": "79988-002-05", "marketing_start_date": "20250106"}, {"sample": false, "description": "50 mL in 1 BOTTLE (79988-002-50)", "package_ndc": "79988-002-50", "marketing_start_date": "20250106"}], "brand_name": "Advanced Day Ultimate Protect Sunscreen SPF 50", "product_id": "79988-002_29071920-ba91-871a-e063-6294a90aee27", "dosage_form": "CREAM", "product_ndc": "79988-002", "generic_name": "Butyl Methoxydibenzoylmethane, Ethylhexyl Salicylate", "labeler_name": "Medik8 Limited", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Advanced Day Ultimate Protect Sunscreen SPF 50", "active_ingredients": [{"name": "BUTYL METHOXYDIBENZOYLMETHANE", "strength": "2.8 g/100mL"}, {"name": "ETHYLHEXYL SALICYLATE", "strength": "4.8 g/100mL"}, {"name": "HOMOSALATE", "strength": "10 g/100mL"}, {"name": "OCTOCRYLENE", "strength": "9.5 g/100mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250106", "listing_expiration_date": "20261231"}