skinceuticals physical uv defense broad spectrum spf 30 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 skinceuticals physical uv defense broad spectrum spf 30 sunscreen
Generic Name titanium dioxide and zinc oxide
Labeler l'oreal usa products inc
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

titanium dioxide 50 mg/mL, zinc oxide 40 mg/mL

Manufacturer
L'Oreal USA Products Inc

Identifiers & Regulatory

Product NDC 49967-472
Product ID 49967-472_fb7295ff-7c8f-4fde-951d-90b68f53e43c
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2012-01-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 49967472
Hyphenated Format 49967-472

Supplemental Identifiers

UPC
0883140024729
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 skinceuticals physical uv defense broad spectrum spf 30 sunscreen (source: ndc)
Generic Name titanium dioxide and zinc oxide (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/mL
  • 40 mg/mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (49967-472-01) / 50 mL in 1 BOTTLE
  • 4 mL in 1 TUBE (49967-472-02)
source: ndc

Packages (2)

49967-472-01 1 BOTTLE in 1 CARTON (49967-472-01) / 50 mL in 1 BOTTLE 49967-472-02 4 mL in 1 TUBE (49967-472-02)

Ingredients (2)

titanium dioxide (50 mg/mL) zinc oxide (40 mg/mL)

Linked Drug Pages (1)

SkinCeuticals Physical UV Defense Broad Spectrum SPF 30 Sunscreen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "fb7295ff-7c8f-4fde-951d-90b68f53e43c", "openfda": {"upc": ["0883140024729"], "unii": ["15FIX9V2JP", "SOI2LOH54Z"], "spl_set_id": ["3a6db7d3-6c59-4633-a97e-1c03127246d3"], "manufacturer_name": ["L'Oreal USA Products Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (49967-472-01)  / 50 mL in 1 BOTTLE", "package_ndc": "49967-472-01", "marketing_start_date": "20120101"}, {"sample": false, "description": "4 mL in 1 TUBE (49967-472-02)", "package_ndc": "49967-472-02", "marketing_start_date": "20120101"}], "brand_name": "SkinCeuticals Physical UV Defense Broad Spectrum SPF 30 Sunscreen", "product_id": "49967-472_fb7295ff-7c8f-4fde-951d-90b68f53e43c", "dosage_form": "CREAM", "product_ndc": "49967-472", "generic_name": "Titanium Dioxide and Zinc Oxide", "labeler_name": "L'Oreal USA Products Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SkinCeuticals Physical UV Defense Broad Spectrum SPF 30 Sunscreen", "active_ingredients": [{"name": "TITANIUM DIOXIDE", "strength": "50 mg/mL"}, {"name": "ZINC OXIDE", "strength": "40 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120101", "listing_expiration_date": "20261231"}