artistry ideal radiance illuminating cc spf 50 broad spectrum sunscreen light/medium

Generic: ensulizole,octinoxate, oxybenzone, titanium dioxide, zinc oxide

Labeler: amway corp
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name artistry ideal radiance illuminating cc spf 50 broad spectrum sunscreen light/medium
Generic Name ensulizole,octinoxate, oxybenzone, titanium dioxide, zinc oxide
Labeler amway corp
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

ensulizole 20 mg/mL, octinoxate 55 mg/mL, oxybenzone 5 mg/mL, titanium dioxide 8.8 mg/mL, zinc oxide 98 mg/mL

Manufacturer
Amway Corp

Identifiers & Regulatory

Product NDC 50390-001
Product ID 50390-001_08370288-7313-b684-e063-6294a90ad541
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2015-05-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50390001
Hyphenated Format 50390-001

Supplemental Identifiers

UNII
9YQ9DI1W42 4Y5P7MUD51 95OOS7VE0Y 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 artistry ideal radiance illuminating cc spf 50 broad spectrum sunscreen light/medium (source: ndc)
Generic Name ensulizole,octinoxate, oxybenzone, titanium dioxide, zinc oxide (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
  • 55 mg/mL
  • 5 mg/mL
  • 8.8 mg/mL
  • 98 mg/mL
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (50390-001-30) / 30 mL in 1 TUBE
source: ndc

Packages (1)

50390-001-30 1 TUBE in 1 CARTON (50390-001-30) / 30 mL in 1 TUBE

Ingredients (5)

ensulizole (20 mg/mL) octinoxate (55 mg/mL) oxybenzone (5 mg/mL) titanium dioxide (8.8 mg/mL) zinc oxide (98 mg/mL)

Linked Drug Pages (1)

Artistry Ideal Radiance Illuminating CC SPF 50 Broad Spectrum Sunscreen Light/Medium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "08370288-7313-b684-e063-6294a90ad541", "openfda": {"unii": ["9YQ9DI1W42", "4Y5P7MUD51", "95OOS7VE0Y", "15FIX9V2JP", "SOI2LOH54Z"], "spl_set_id": ["830a748f-bb14-47f6-ab6f-48d8bd706321"], "manufacturer_name": ["Amway Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (50390-001-30)  / 30 mL in 1 TUBE", "package_ndc": "50390-001-30", "marketing_start_date": "20150501"}], "brand_name": "Artistry Ideal Radiance Illuminating CC SPF 50 Broad Spectrum Sunscreen Light/Medium", "product_id": "50390-001_08370288-7313-b684-e063-6294a90ad541", "dosage_form": "CREAM", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "50390-001", "generic_name": "ENSULIZOLE,OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, ZINC OXIDE", "labeler_name": "Amway Corp", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Artistry Ideal Radiance Illuminating CC SPF 50 Broad Spectrum Sunscreen Light/Medium", "active_ingredients": [{"name": "ENSULIZOLE", "strength": "20 mg/mL"}, {"name": "OCTINOXATE", "strength": "55 mg/mL"}, {"name": "OXYBENZONE", "strength": "5 mg/mL"}, {"name": "TITANIUM DIOXIDE", "strength": "8.8 mg/mL"}, {"name": "ZINC OXIDE", "strength": "98 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150501", "listing_expiration_date": "20261231"}