la roche posay laboratoire dermatologique anthelios tinted mineral light fluid sunscreen broad spectrum spf 40 medium

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 tinted mineral light fluid sunscreen broad spectrum spf 40 medium
Generic Name titanium dioxide and zinc oxide
Labeler l'oreal usa products inc
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

titanium dioxide 170 mg/mL, zinc oxide 80 mg/mL

Manufacturer
L'Oreal USA Products Inc

Identifiers & Regulatory

Product NDC 49967-210
Product ID 49967-210_de458c44-6b00-481b-a1ab-c9c00ae07d96
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2023-12-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 49967210
Hyphenated Format 49967-210

Supplemental Identifiers

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 tinted mineral light fluid sunscreen broad spectrum spf 40 medium (source: ndc)
Generic Name titanium dioxide and zinc oxide (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 170 mg/mL
  • 80 mg/mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (49967-210-01) / 50 mL in 1 BOTTLE
  • 1 TUBE in 1 CARTON (49967-210-02) / 5 mL in 1 TUBE
source: ndc

Packages (2)

Ingredients (2)

titanium dioxide (170 mg/mL) zinc oxide (80 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "de458c44-6b00-481b-a1ab-c9c00ae07d96", "openfda": {"unii": ["15FIX9V2JP", "SOI2LOH54Z"], "spl_set_id": ["1f3b56d5-c33a-401f-8c8a-924345a4846e"], "manufacturer_name": ["L'Oreal USA Products Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (49967-210-01)  / 50 mL in 1 BOTTLE", "package_ndc": "49967-210-01", "marketing_start_date": "20231215"}, {"sample": false, "description": "1 TUBE in 1 CARTON (49967-210-02)  / 5 mL in 1 TUBE", "package_ndc": "49967-210-02", "marketing_start_date": "20231215"}], "brand_name": "La Roche Posay Laboratoire Dermatologique Anthelios Tinted Mineral Light Fluid Sunscreen Broad Spectrum SPF 40 Medium", "product_id": "49967-210_de458c44-6b00-481b-a1ab-c9c00ae07d96", "dosage_form": "LOTION", "product_ndc": "49967-210", "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 Anthelios Tinted Mineral Light Fluid Sunscreen Broad Spectrum SPF 40 Medium", "active_ingredients": [{"name": "TITANIUM DIOXIDE", "strength": "170 mg/mL"}, {"name": "ZINC OXIDE", "strength": "80 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20231215", "listing_expiration_date": "20261231"}