skinceuticals physical eye uv defense 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 eye uv defense sunscreen
Generic Name titanium dioxide and zinc oxide
Labeler l'oreal usa products inc
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

titanium dioxide 90 mg/mL, zinc oxide 40 mg/mL

Manufacturer
L'Oreal USA Products Inc

Identifiers & Regulatory

Product NDC 49967-050
Product ID 49967-050_d62bc8a0-0a64-4200-9549-d112826a1646
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Marketing Start 2014-04-18
Marketing End 2026-07-27

Pharmacologic Class

Classes
copper absorption inhibitor [epc] decreased copper ion absorption [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 49967050
Hyphenated Format 49967-050

Supplemental Identifiers

UPC
3606000400504
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 eye uv defense sunscreen (source: ndc)
Generic Name titanium dioxide and zinc oxide (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 90 mg/mL
  • 40 mg/mL
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (49967-050-01) / 10 mL in 1 TUBE
  • .15 mL in 1 PACKET (49967-050-02)
source: ndc

Packages (2)

49967-050-01 1 TUBE in 1 CARTON (49967-050-01) / 10 mL in 1 TUBE 49967-050-02 .15 mL in 1 PACKET (49967-050-02)

Ingredients (2)

titanium dioxide (90 mg/mL) zinc oxide (40 mg/mL)

Linked Drug Pages (1)

SkinCeuticals Physical Eye UV Defense Sunscreen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "d62bc8a0-0a64-4200-9549-d112826a1646", "openfda": {"upc": ["3606000400504"], "unii": ["15FIX9V2JP", "SOI2LOH54Z"], "spl_set_id": ["5fb2ec75-6d79-4b06-839c-2e0976309942"], "manufacturer_name": ["L'Oreal USA Products Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (49967-050-01)  / 10 mL in 1 TUBE", "package_ndc": "49967-050-01", "marketing_end_date": "20260727", "marketing_start_date": "20140418"}, {"sample": false, "description": ".15 mL in 1 PACKET (49967-050-02)", "package_ndc": "49967-050-02", "marketing_end_date": "20260727", "marketing_start_date": "20140418"}], "brand_name": "SkinCeuticals Physical Eye UV Defense Sunscreen", "product_id": "49967-050_d62bc8a0-0a64-4200-9549-d112826a1646", "dosage_form": "LOTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "49967-050", "generic_name": "Titanium dioxide and Zinc oxide", "labeler_name": "L'Oreal USA Products Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SkinCeuticals Physical Eye UV Defense Sunscreen", "active_ingredients": [{"name": "TITANIUM DIOXIDE", "strength": "90 mg/mL"}, {"name": "ZINC OXIDE", "strength": "40 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20260727", "marketing_start_date": "20140418"}