Pro-Tect Everyday Sunscreen SPF 15 is a Topical Lotion in the Human Otc Drug category. It is labeled and distributed by Bio-medical & Pharmaceutical Manufacturing Corporation. The primary component is Octinoxate; Oxybenzone; Padimate O.
| Product ID | 37945-868_0eae8a83-5536-5611-e054-00144ff88e88 |
| NDC | 37945-868 |
| Product Type | Human Otc Drug |
| Proprietary Name | Pro-Tect Everyday Sunscreen SPF 15 |
| Generic Name | Octinoxate, Octisalate, Padimate O |
| Dosage Form | Lotion |
| Route of Administration | TOPICAL |
| Marketing Start Date | 1987-12-01 |
| Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
| Application Number | part352 |
| Labeler Name | Bio-Medical & Pharmaceutical Manufacturing Corporation |
| Substance Name | OCTINOXATE; OXYBENZONE; PADIMATE O |
| Active Ingredient Strength | 75 mg/g; mg/g; mg/g |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
| Marketing Start Date | 2015-07-20 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 1987-12-01 |
| Marketing End Date | 2015-02-05 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2015-07-20 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2015-02-05 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| OCTINOXATE | 75 mg/g |
| SPL SET ID: | 1a3b3924-c01b-01da-e054-00144ff88e88 |
| Manufacturer | |
| UNII |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 61619-868 | PRO-TECT EVERYDAY SUNSCREEN SPF 15 | Octinoxate, Octisalate, Padimate O |
| 37945-868 | Pro-Tect Everyday Sunscreen | Octinoxate, Octisalate, Padimate O |