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NDC 50390-0108-30 ARTISTRY IDEAL RADIANCE UV Protect SPF 50 PLUS Broad Spectrum Sunscreen 68; 45; 24.9; 126.6 mg/mL; mg/mL; mg/mL; mg/mL Details
ARTISTRY IDEAL RADIANCE UV Protect SPF 50 PLUS Broad Spectrum Sunscreen 68; 45; 24.9; 126.6 mg/mL; mg/mL; mg/mL; mg/mL
ARTISTRY IDEAL RADIANCE UV Protect SPF 50 PLUS Broad Spectrum Sunscreen is a TOPICAL CREAM in the HUMAN OTC DRUG category. It is labeled and distributed by Amway Corp. The primary component is OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE; ZINC OXIDE.
Product Information
| NDC | 50390-0108 |
|---|---|
| Product ID | 50390-108_0daad476-bd32-bd5d-e063-6394a90ac74a |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | ARTISTRY IDEAL RADIANCE UV Protect SPF 50 PLUS Broad Spectrum Sunscreen |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | OCTINOXATE, OCTISALATE, ZINC OXIDE, TITANIUM DIOXIDE |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | CREAM |
| Route | TOPICAL |
| Active Ingredient Strength | 68; 45; 24.9; 126.6 |
| Active Ingredient Units | mg/mL; mg/mL; mg/mL; mg/mL |
| Substance Name | OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Labeler Name | Amway Corp |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH DRUG |
| Application Number | M020 |
| Listing Certified Through | 2025-12-31 |
Package
NDC 50390-0108-30 (50390010830)
| NDC Package Code | 50390-108-30 |
|---|---|
| Billing NDC | 50390010830 |
| Package | 1 BOTTLE in 1 CARTON (50390-108-30) / 30 mL in 1 BOTTLE |
| Marketing Start Date | 2013-09-11 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |