la roche posay laboratoire dermatologique anthelios 50 mineral ultra light broad spectrum spf 50 sunscreen

Generic: titanium dioxide and zinc oxide

Labeler: cosmetique active production
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name la roche posay laboratoire dermatologique anthelios 50 mineral ultra light broad spectrum spf 50 sunscreen
Generic Name titanium dioxide and zinc oxide
Labeler cosmetique active production
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

titanium dioxide 60 mg/mL, zinc oxide 50 mg/mL

Manufacturer
Cosmetique Active Production

Identifiers & Regulatory

Product NDC 69625-908
Product ID 69625-908_52bd923b-28c8-4baf-afca-eeac9d5adb70
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2011-07-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69625908
Hyphenated Format 69625-908

Supplemental Identifiers

UPC
0883140000907
UNII
15FIX9V2JP 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 la roche posay laboratoire dermatologique anthelios 50 mineral ultra light broad spectrum spf 50 sunscreen (source: ndc)
Generic Name titanium dioxide and zinc oxide (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 60 mg/mL
  • 50 mg/mL
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (69625-908-01) / 50 mL in 1 BOTTLE, PLASTIC
  • 1 TUBE in 1 CARTON (69625-908-03) / 5 mL in 1 TUBE
source: ndc

Packages (2)

Ingredients (2)

titanium dioxide (60 mg/mL) zinc oxide (50 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "52bd923b-28c8-4baf-afca-eeac9d5adb70", "openfda": {"upc": ["0883140000907"], "unii": ["15FIX9V2JP", "SOI2LOH54Z"], "spl_set_id": ["4e56f3f2-b856-4bbc-ab39-6fb5887a4846"], "manufacturer_name": ["Cosmetique Active Production"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (69625-908-01)  / 50 mL in 1 BOTTLE, PLASTIC", "package_ndc": "69625-908-01", "marketing_start_date": "20110701"}, {"sample": false, "description": "1 TUBE in 1 CARTON (69625-908-03)  / 5 mL in 1 TUBE", "package_ndc": "69625-908-03", "marketing_start_date": "20191202"}], "brand_name": "La Roche Posay Laboratoire Dermatologique Anthelios 50 Mineral Ultra Light Broad Spectrum SPF 50 Sunscreen", "product_id": "69625-908_52bd923b-28c8-4baf-afca-eeac9d5adb70", "dosage_form": "LOTION", "product_ndc": "69625-908", "generic_name": "Titanium dioxide and Zinc oxide", "labeler_name": "Cosmetique Active Production", "product_type": "HUMAN OTC DRUG", "brand_name_base": "La Roche Posay Laboratoire Dermatologique Anthelios 50 Mineral Ultra Light Broad Spectrum SPF 50 Sunscreen", "active_ingredients": [{"name": "TITANIUM DIOXIDE", "strength": "60 mg/mL"}, {"name": "ZINC OXIDE", "strength": "50 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20110701", "listing_expiration_date": "20261231"}