la roche posay laboratoire dermatologique anthelios 50 tinted mineral sunscreen

Generic: titanium dioxide

Labeler: l'oreal usa products inc
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
Generic Name titanium dioxide
Labeler l'oreal usa products inc
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

titanium dioxide 110 mg/mL

Manufacturer
L'Oreal USA Products Inc

Identifiers & Regulatory

Product NDC 49967-899
Product ID 49967-899_2af1e670-d87a-423c-a0dc-9aac07b4166a
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 49967899
Hyphenated Format 49967-899

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 (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 (49967-899-01) / 50 mL in 1 BOTTLE, PLASTIC
  • 1 TUBE in 1 CARTON (49967-899-02) / 3 mL in 1 TUBE
  • 1 BOTTLE in 1 CARTON (49967-899-03) / 125 mL in 1 BOTTLE
source: ndc

Packages (3)

49967-899-01 1 BOTTLE, PLASTIC in 1 CARTON (49967-899-01) / 50 mL in 1 BOTTLE, PLASTIC 49967-899-02 1 TUBE in 1 CARTON (49967-899-02) / 3 mL in 1 TUBE 49967-899-03 1 BOTTLE in 1 CARTON (49967-899-03) / 125 mL in 1 BOTTLE

Ingredients (1)

titanium dioxide (110 mg/mL)

Linked Drug Pages (1)

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

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "2af1e670-d87a-423c-a0dc-9aac07b4166a", "openfda": {"upc": ["0883740020299"], "unii": ["15FIX9V2JP"], "spl_set_id": ["6d3c5fc5-c818-46c4-8db3-cffcdcd56e06"], "manufacturer_name": ["L'Oreal USA Products Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (49967-899-01)  / 50 mL in 1 BOTTLE, PLASTIC", "package_ndc": "49967-899-01", "marketing_start_date": "20120601"}, {"sample": false, "description": "1 TUBE in 1 CARTON (49967-899-02)  / 3 mL in 1 TUBE", "package_ndc": "49967-899-02", "marketing_start_date": "20120601"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (49967-899-03)  / 125 mL in 1 BOTTLE", "package_ndc": "49967-899-03", "marketing_start_date": "20120601"}], "brand_name": "La Roche Posay Laboratoire Dermatologique Anthelios 50 Tinted Mineral Sunscreen", "product_id": "49967-899_2af1e670-d87a-423c-a0dc-9aac07b4166a", "dosage_form": "LOTION", "product_ndc": "49967-899", "generic_name": "Titanium Dioxide", "labeler_name": "L'Oreal USA Products Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "La Roche Posay Laboratoire Dermatologique", "brand_name_suffix": "Anthelios 50 Tinted Mineral Sunscreen", "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"}