shiseido uv protective compact (refill) medium beige

Generic: octinoxate, octocrylene, and titanium dioxide

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

Drug Facts

Product Profile

Brand Name shiseido uv protective compact (refill) medium beige
Generic Name octinoxate, octocrylene, and titanium dioxide
Labeler shiseido americas corporation
Dosage Form POWDER
Routes
TOPICAL
Active Ingredients

octinoxate 888 mg/12g, octocrylene 600 mg/12g, titanium dioxide 1416 mg/12g

Manufacturer
SHISEIDO AMERICAS CORPORATION

Identifiers & Regulatory

Product NDC 58411-125
Product ID 58411-125_4ba6bd60-913b-4748-e063-6394a90aed10
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2027-12-31
Marketing Start 2014-02-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 58411125
Hyphenated Format 58411-125

Supplemental Identifiers

UNII
4Y5P7MUD51 15FIX9V2JP 5A68WGF6WM

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 uv protective compact (refill) medium beige (source: ndc)
Generic Name octinoxate, octocrylene, and titanium dioxide (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 888 mg/12g
  • 600 mg/12g
  • 1416 mg/12g
source: ndc
Packaging
  • 1 TRAY in 1 CARTON (58411-125-30) / 12 g in 1 TRAY
source: ndc

Packages (1)

58411-125-30 1 TRAY in 1 CARTON (58411-125-30) / 12 g in 1 TRAY

Ingredients (3)

octinoxate (888 mg/12g) octocrylene (600 mg/12g) titanium dioxide (1416 mg/12g)

Linked Drug Pages (1)

SHISEIDO UV PROTECTIVE COMPACT (REFILL) MEDIUM BEIGE, SHISEIDO UV PROTECTIVE COMPACT (REFILL) MEDIUM IVORY, SHISEIDO UV PROTECTIVE COMPACT (REFILL) MEDIUM OCHRE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "4ba6bd60-913b-4748-e063-6394a90aed10", "openfda": {"unii": ["4Y5P7MUD51", "15FIX9V2JP", "5A68WGF6WM"], "spl_set_id": ["c05cef12-a6a7-4682-9357-6d77f4ca3267"], "manufacturer_name": ["SHISEIDO AMERICAS CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TRAY in 1 CARTON (58411-125-30)  / 12 g in 1 TRAY", "package_ndc": "58411-125-30", "marketing_start_date": "20140201"}], "brand_name": "SHISEIDO UV PROTECTIVE COMPACT (REFILL) MEDIUM BEIGE", "product_id": "58411-125_4ba6bd60-913b-4748-e063-6394a90aed10", "dosage_form": "POWDER", "product_ndc": "58411-125", "generic_name": "OCTINOXATE, OCTOCRYLENE, and TITANIUM DIOXIDE", "labeler_name": "SHISEIDO AMERICAS CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SHISEIDO UV PROTECTIVE COMPACT (REFILL)", "brand_name_suffix": "MEDIUM BEIGE", "active_ingredients": [{"name": "OCTINOXATE", "strength": "888 mg/12g"}, {"name": "OCTOCRYLENE", "strength": "600 mg/12g"}, {"name": "TITANIUM DIOXIDE", "strength": "1416 mg/12g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20140201", "listing_expiration_date": "20271231"}