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NDC 59088-0568-05 DermacinRx Skin Moisturizing Ultra SPF 50 Sunscreen 25; 30; 30; 12.5 mg/mL; mg/mL; mg/mL; mg/mL Details
DermacinRx Skin Moisturizing Ultra SPF 50 Sunscreen 25; 30; 30; 12.5 mg/mL; mg/mL; mg/mL; mg/mL
DermacinRx Skin Moisturizing Ultra SPF 50 Sunscreen is a TOPICAL LOTION in the HUMAN OTC DRUG category. It is labeled and distributed by PureTek Corporation. The primary component is AVOBENZONE; OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE.
Product Information
| NDC | 59088-0568 |
|---|---|
| Product ID | 59088-568_f20534c0-4cbf-31f7-e053-2995a90a6879 |
| 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 | DermacinRx Skin Moisturizing Ultra SPF 50 Sunscreen |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | avobenzone, octinoxate, octisalate, titanium dioxide |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | LOTION |
| Route | TOPICAL |
| Active Ingredient Strength | 25; 30; 30; 12.5 |
| Active Ingredient Units | mg/mL; mg/mL; mg/mL; mg/mL |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE |
| Labeler Name | PureTek Corporation |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part352 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 59088-0568-05 (59088056805)
| NDC Package Code | 59088-568-05 |
|---|---|
| Billing NDC | 59088056805 |
| Package | 56 mL in 1 BOTTLE (59088-568-05) |
| Marketing Start Date | 2017-02-16 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |