artistry ideal radiance uv protect spf 50 plus broad spectrum sunscreen

Generic: octinoxate, octisalate, zinc oxide, titanium dioxide

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

Drug Facts

Product Profile

Brand Name artistry ideal radiance uv protect spf 50 plus broad spectrum sunscreen
Generic Name octinoxate, octisalate, zinc oxide, titanium dioxide
Labeler amway corp
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

octinoxate 68 mg/mL, octisalate 45 mg/mL, titanium dioxide 24.9 mg/mL, zinc oxide 126.6 mg/mL

Manufacturer
Amway Corp

Identifiers & Regulatory

Product NDC 50390-108
Product ID 50390-108_0daad476-bd32-bd5d-e063-6394a90ac74a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2013-09-11

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50390108
Hyphenated Format 50390-108

Supplemental Identifiers

UNII
4Y5P7MUD51 4X49Y0596W 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 uv protect spf 50 plus broad spectrum sunscreen (source: ndc)
Generic Name octinoxate, octisalate, zinc oxide, titanium dioxide (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 68 mg/mL
  • 45 mg/mL
  • 24.9 mg/mL
  • 126.6 mg/mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (50390-108-30) / 30 mL in 1 BOTTLE
source: ndc

Packages (1)

50390-108-30 1 BOTTLE in 1 CARTON (50390-108-30) / 30 mL in 1 BOTTLE

Ingredients (4)

octinoxate (68 mg/mL) octisalate (45 mg/mL) titanium dioxide (24.9 mg/mL) zinc oxide (126.6 mg/mL)

Linked Drug Pages (1)

ARTISTRY IDEAL RADIANCE UV Protect SPF 50 PLUS Broad Spectrum Sunscreen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "0daad476-bd32-bd5d-e063-6394a90ac74a", "openfda": {"unii": ["4Y5P7MUD51", "4X49Y0596W", "15FIX9V2JP", "SOI2LOH54Z"], "spl_set_id": ["a1a700b5-d039-4bd2-8420-5c2053095706"], "manufacturer_name": ["Amway Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (50390-108-30)  / 30 mL in 1 BOTTLE", "package_ndc": "50390-108-30", "marketing_start_date": "20130911"}], "brand_name": "ARTISTRY IDEAL RADIANCE UV Protect SPF 50 PLUS Broad Spectrum Sunscreen", "product_id": "50390-108_0daad476-bd32-bd5d-e063-6394a90ac74a", "dosage_form": "CREAM", "product_ndc": "50390-108", "generic_name": "OCTINOXATE, OCTISALATE, ZINC OXIDE, TITANIUM DIOXIDE", "labeler_name": "Amway Corp", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ARTISTRY IDEAL RADIANCE UV Protect SPF 50 PLUS Broad Spectrum Sunscreen", "active_ingredients": [{"name": "OCTINOXATE", "strength": "68 mg/mL"}, {"name": "OCTISALATE", "strength": "45 mg/mL"}, {"name": "TITANIUM DIOXIDE", "strength": "24.9 mg/mL"}, {"name": "ZINC OXIDE", "strength": "126.6 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20130911", "listing_expiration_date": "20261231"}