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

Generic: titanium dioxide

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 tinted mineral sunscreen broad spectrum spf 50
Generic Name titanium dioxide
Labeler cosmetique active production
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

titanium dioxide 110 mg/mL

Manufacturer
Cosmetique Active Production

Identifiers & Regulatory

Product NDC 69625-899
Product ID 69625-899_7b757c3c-a037-491c-99a0-b9c60d31d452
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2012-06-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69625899
Hyphenated Format 69625-899

Supplemental Identifiers

UPC
0883740020299
UNII
15FIX9V2JP

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 tinted mineral sunscreen broad spectrum spf 50 (source: ndc)
Generic Name titanium dioxide (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 110 mg/mL
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (69625-899-01) / 50 mL in 1 BOTTLE, PLASTIC
  • 1 TUBE in 1 CARTON (69625-899-02) / 3 mL in 1 TUBE
source: ndc

Packages (2)

69625-899-01 1 BOTTLE, PLASTIC in 1 CARTON (69625-899-01) / 50 mL in 1 BOTTLE, PLASTIC 69625-899-02 1 TUBE in 1 CARTON (69625-899-02) / 3 mL in 1 TUBE

Ingredients (1)

titanium dioxide (110 mg/mL)

Linked Drug Pages (1)

La Roche Posay Laboratoire Dermatologique Anthelios 50 Tinted Mineral Sunscreen Broad Spectrum SPF 50 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "7b757c3c-a037-491c-99a0-b9c60d31d452", "openfda": {"upc": ["0883740020299"], "unii": ["15FIX9V2JP"], "spl_set_id": ["fd2541e1-c409-40a8-9e3f-6ff69084ea66"], "manufacturer_name": ["Cosmetique Active Production"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (69625-899-01)  / 50 mL in 1 BOTTLE, PLASTIC", "package_ndc": "69625-899-01", "marketing_start_date": "20120601"}, {"sample": false, "description": "1 TUBE in 1 CARTON (69625-899-02)  / 3 mL in 1 TUBE", "package_ndc": "69625-899-02", "marketing_start_date": "20120601"}], "brand_name": "La Roche Posay Laboratoire Dermatologique Anthelios 50 Tinted Mineral Sunscreen Broad Spectrum SPF 50", "product_id": "69625-899_7b757c3c-a037-491c-99a0-b9c60d31d452", "dosage_form": "LOTION", "product_ndc": "69625-899", "generic_name": "Titanium Dioxide", "labeler_name": "Cosmetique Active Production", "product_type": "HUMAN OTC DRUG", "brand_name_base": "La Roche Posay Laboratoire Dermatologique Anthelios 50 Tinted Mineral Sunscreen Broad Spectrum SPF 50", "active_ingredients": [{"name": "TITANIUM DIOXIDE", "strength": "110 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120601", "listing_expiration_date": "20261231"}