shiseido white lucent day

Generic: avobenzone, octinoxate, and octocrylene

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

Drug Facts

Product Profile

Brand Name shiseido white lucent day
Generic Name avobenzone, octinoxate, and octocrylene
Labeler shiseido americas corporation
Dosage Form EMULSION
Routes
TOPICAL
Active Ingredients

avobenzone 1.285 g/50mL, octinoxate 3.8036 g/50mL, octocrylene 1.542 g/50mL

Manufacturer
SHISEIDO AMERICAS CORPORATION

Identifiers & Regulatory

Product NDC 58411-463
Product ID 58411-463_47ba6cbd-e2e4-a60e-e063-6394a90ab02a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2027-12-31
Marketing Start 2019-01-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 58411463
Hyphenated Format 58411-463

Supplemental Identifiers

UNII
G63QQF2NOX 4Y5P7MUD51 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 white lucent day (source: ndc)
Generic Name avobenzone, octinoxate, and octocrylene (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 1.285 g/50mL
  • 3.8036 g/50mL
  • 1.542 g/50mL
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (58411-463-10) / 50 mL in 1 TUBE
source: ndc

Packages (1)

58411-463-10 1 TUBE in 1 CARTON (58411-463-10) / 50 mL in 1 TUBE

Ingredients (3)

avobenzone (1.285 g/50mL) octinoxate (3.8036 g/50mL) octocrylene (1.542 g/50mL)

Linked Drug Pages (1)

SHISEIDO WHITE LUCENT DAY ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "47ba6cbd-e2e4-a60e-e063-6394a90ab02a", "openfda": {"unii": ["G63QQF2NOX", "4Y5P7MUD51", "5A68WGF6WM"], "spl_set_id": ["e881e637-e0f0-4c90-8343-2be6e74020b8"], "manufacturer_name": ["SHISEIDO AMERICAS CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (58411-463-10)  / 50 mL in 1 TUBE", "package_ndc": "58411-463-10", "marketing_start_date": "20190101"}], "brand_name": "SHISEIDO WHITE LUCENT DAY", "product_id": "58411-463_47ba6cbd-e2e4-a60e-e063-6394a90ab02a", "dosage_form": "EMULSION", "product_ndc": "58411-463", "generic_name": "AVOBENZONE, OCTINOXATE, and OCTOCRYLENE", "labeler_name": "SHISEIDO AMERICAS CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SHISEIDO WHITE LUCENT DAY", "active_ingredients": [{"name": "AVOBENZONE", "strength": "1.285 g/50mL"}, {"name": "OCTINOXATE", "strength": "3.8036 g/50mL"}, {"name": "OCTOCRYLENE", "strength": "1.542 g/50mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190101", "listing_expiration_date": "20271231"}