la roche posay laboratoire dermatologique anthelios 50 mineral ultra light sunscreen

Generic: titanium dioxide and zinc oxide

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 mineral ultra light sunscreen
Generic Name titanium dioxide and zinc oxide
Labeler l'oreal usa products inc
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

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

Manufacturer
L'Oreal USA Products Inc

Identifiers & Regulatory

Product NDC 49967-907
Product ID 49967-907_93f2cacd-67af-4ad8-9e0a-4de8330f808f
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 49967907
Hyphenated Format 49967-907

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 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 (49967-907-01) / 50 mL in 1 BOTTLE, PLASTIC
  • 1 TUBE in 1 CARTON (49967-907-03) / 5 mL in 1 TUBE
source: ndc

Packages (2)

49967-907-01 1 BOTTLE, PLASTIC in 1 CARTON (49967-907-01) / 50 mL in 1 BOTTLE, PLASTIC 49967-907-03 1 TUBE in 1 CARTON (49967-907-03) / 5 mL in 1 TUBE

Ingredients (2)

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

Linked Drug Pages (1)

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

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "93f2cacd-67af-4ad8-9e0a-4de8330f808f", "openfda": {"upc": ["0883140000907"], "unii": ["15FIX9V2JP", "SOI2LOH54Z"], "spl_set_id": ["2ce83dc2-84b6-43fd-8b11-495d41cebc22"], "manufacturer_name": ["L'Oreal USA Products Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (49967-907-01)  / 50 mL in 1 BOTTLE, PLASTIC", "package_ndc": "49967-907-01", "marketing_start_date": "20110701"}, {"sample": false, "description": "1 TUBE in 1 CARTON (49967-907-03)  / 5 mL in 1 TUBE", "package_ndc": "49967-907-03", "marketing_start_date": "20191202"}], "brand_name": "La Roche Posay Laboratoire Dermatologique Anthelios 50 Mineral Ultra Light Sunscreen", "product_id": "49967-907_93f2cacd-67af-4ad8-9e0a-4de8330f808f", "dosage_form": "LOTION", "product_ndc": "49967-907", "generic_name": "Titanium dioxide and Zinc oxide", "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 Mineral Ultra Light 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"}