shiseido urban environment

Generic: ensulizole, homosalate, octisalate, zinc oxide

Labeler: shiseido americas corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name shiseido urban environment
Generic Name ensulizole, homosalate, octisalate, zinc oxide
Labeler shiseido americas corporation
Dosage Form EMULSION
Routes
TOPICAL
Active Ingredients

ensulizole .6 g/50mL, homosalate 9 g/50mL, octisalate 3 g/50mL, zinc oxide 9.3 g/50mL

Manufacturer
Shiseido Americas Corporation

Identifiers & Regulatory

Product NDC 58411-952
Product ID 58411-952_4617da57-c5ae-99fc-e063-6394a90ac726
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2025-12-11

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 58411952
Hyphenated Format 58411-952

Supplemental Identifiers

UNII
9YQ9DI1W42 V06SV4M95S 4X49Y0596W 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 shiseido urban environment (source: ndc)
Generic Name ensulizole, homosalate, octisalate, zinc oxide (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • .6 g/50mL
  • 9 g/50mL
  • 3 g/50mL
  • 9.3 g/50mL
source: ndc
Packaging
  • SHISEIDO Ginza Tokyo Urban Environment Sun Dual Care OIL-FREE with HYALURONIC ACID SPF 42 BROAD SPECTRUM SPF 42 WATER RESISTANT (40 MINUTES) SUNSCREEN 50mL 1.6 FL. OZ. urban environment oil free label
source: label

Packages (0)

No package records.

Ingredients (4)

ensulizole (.6 g/50mL) homosalate (9 g/50mL) octisalate (3 g/50mL) zinc oxide (9.3 g/50mL)

Linked Drug Pages (1)

SHISEIDO URBAN ENVIRONMENT ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "4617da57-c5ae-99fc-e063-6394a90ac726", "openfda": {"unii": ["9YQ9DI1W42", "V06SV4M95S", "4X49Y0596W", "SOI2LOH54Z"], "spl_set_id": ["8db9f5e0-a8d6-4872-b4c6-cb92c43d25c2"], "manufacturer_name": ["Shiseido Americas Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [], "brand_name": "SHISEIDO URBAN ENVIRONMENT", "product_id": "58411-952_4617da57-c5ae-99fc-e063-6394a90ac726", "dosage_form": "EMULSION", "product_ndc": "58411-952", "generic_name": "Ensulizole, Homosalate, Octisalate, Zinc OXide", "labeler_name": "Shiseido Americas Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SHISEIDO URBAN ENVIRONMENT", "active_ingredients": [{"name": "ENSULIZOLE", "strength": ".6 g/50mL"}, {"name": "HOMOSALATE", "strength": "9 g/50mL"}, {"name": "OCTISALATE", "strength": "3 g/50mL"}, {"name": "ZINC OXIDE", "strength": "9.3 g/50mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251211", "listing_expiration_date": "20261231"}