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NDC 50390-0011-00 Artistry Ideal Radiance Illuminating CC SPF 50 Broad Spectrum Med/Deep 20; 55; 5; 84; 98 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL Details
Artistry Ideal Radiance Illuminating CC SPF 50 Broad Spectrum Med/Deep 20; 55; 5; 84; 98 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL
Artistry Ideal Radiance Illuminating CC SPF 50 Broad Spectrum Med/Deep is a TOPICAL CREAM in the HUMAN OTC DRUG category. It is labeled and distributed by Amway Corp. The primary component is ENSULIZOLE; OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE; ZINC OXIDE.
Product Information
| NDC | 50390-0011 |
|---|---|
| Product ID | 50390-011_0837488b-c5e4-34c6-e063-6294a90aca13 |
| 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 Illuminating CC SPF 50 Broad Spectrum Med/Deep |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | ENSULIZOLE, OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, ZINC OXIDE |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | CREAM |
| Route | TOPICAL |
| Active Ingredient Strength | 20; 55; 5; 84; 98 |
| Active Ingredient Units | mg/mL; mg/mL; mg/mL; mg/mL; mg/mL |
| Substance Name | ENSULIZOLE; OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE; ZINC OXIDE |
| Labeler Name | Amway Corp |
| Pharmaceutical Class | Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE] |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH DRUG |
| Application Number | M020 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 50390-0011-00 (50390001100)
| NDC Package Code | 50390-011-00 |
|---|---|
| Billing NDC | 50390001100 |
| Package | 1 TUBE in 1 CARTON (50390-011-00) / 30 mL in 1 TUBE |
| Marketing Start Date | 2017-09-23 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |