daily prevention ultra defense moisturizer spf 50

Generic: homosalate, octisalate,octocrylene and zinc oxide

Labeler: allure labs
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name daily prevention ultra defense moisturizer spf 50
Generic Name homosalate, octisalate,octocrylene and zinc oxide
Labeler allure labs
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

homosalate 7.3 g/100g, octisalate 5 g/100g, octocrylene 9.9 g/100g, zinc oxide 7 g/100g

Manufacturer
Allure Labs

Identifiers & Regulatory

Product NDC 62742-4255
Product ID 62742-4255_14070076-8c58-e2f1-e063-6394a90a0dfc
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2024-03-19

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 627424255
Hyphenated Format 62742-4255

Supplemental Identifiers

UNII
V06SV4M95S 4X49Y0596W 5A68WGF6WM SOI2LOH54Z

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 daily prevention ultra defense moisturizer spf 50 (source: ndc)
Generic Name homosalate, octisalate,octocrylene and zinc oxide (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 7.3 g/100g
  • 5 g/100g
  • 9.9 g/100g
  • 7 g/100g
source: ndc
Packaging
  • 7 g in 1 TUBE (62742-4255-1)
  • 1 TUBE in 1 CARTON (62742-4255-3) / 73 g in 1 TUBE (62742-4255-2)
  • 142 g in 1 TUBE (62742-4255-4)
source: ndc

Packages (3)

62742-4255-1 7 g in 1 TUBE (62742-4255-1) 62742-4255-3 1 TUBE in 1 CARTON (62742-4255-3) / 73 g in 1 TUBE (62742-4255-2) 62742-4255-4 142 g in 1 TUBE (62742-4255-4)

Ingredients (4)

homosalate (7.3 g/100g) octisalate (5 g/100g) octocrylene (9.9 g/100g) zinc oxide (7 g/100g)

Linked Drug Pages (1)

Daily Prevention Ultra Defense Moisturizer SPF 50 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "14070076-8c58-e2f1-e063-6394a90a0dfc", "openfda": {"unii": ["V06SV4M95S", "4X49Y0596W", "5A68WGF6WM", "SOI2LOH54Z"], "spl_set_id": ["14070076-8c57-e2f1-e063-6394a90a0dfc"], "manufacturer_name": ["Allure Labs"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "7 g in 1 TUBE (62742-4255-1)", "package_ndc": "62742-4255-1", "marketing_start_date": "20240319"}, {"sample": false, "description": "1 TUBE in 1 CARTON (62742-4255-3)  / 73 g in 1 TUBE (62742-4255-2)", "package_ndc": "62742-4255-3", "marketing_start_date": "20240319"}, {"sample": false, "description": "142 g in 1 TUBE (62742-4255-4)", "package_ndc": "62742-4255-4", "marketing_start_date": "20240319"}], "brand_name": "Daily Prevention Ultra Defense Moisturizer SPF 50", "product_id": "62742-4255_14070076-8c58-e2f1-e063-6394a90a0dfc", "dosage_form": "CREAM", "product_ndc": "62742-4255", "generic_name": "Homosalate, Octisalate,Octocrylene and Zinc Oxide", "labeler_name": "Allure Labs", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Daily Prevention Ultra Defense Moisturizer SPF 50", "active_ingredients": [{"name": "HOMOSALATE", "strength": "7.3 g/100g"}, {"name": "OCTISALATE", "strength": "5 g/100g"}, {"name": "OCTOCRYLENE", "strength": "9.9 g/100g"}, {"name": "ZINC OXIDE", "strength": "7 g/100g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240319", "listing_expiration_date": "20261231"}