PRO-TECT EVERYDAY SUNSCREEN SPF 15 is a Topical Lotion in the Human Otc Drug category. It is labeled and distributed by A-cute Derm, Incorporated. The primary component is Octinoxate; Oxybenzone; Padimate O.
Product ID | 61619-868_232cc4ca-790c-2e81-e054-00144ff88e88 |
NDC | 61619-868 |
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 | 2015-11-03 |
Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
Application Number | part352 |
Labeler Name | A-Cute Derm, Incorporated |
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 | 2015-11-03 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-11-03 |
Marketing End Date | 2016-05-04 |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-11-03 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-11-03 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-11-03 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-11-03 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-11-03 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-11-03 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-11-03 |
Inactivation Date | 2020-01-31 |
Ingredient | Strength |
---|---|
OCTINOXATE | 75 mg/g |
SPL SET ID: | 232d7902-e3c5-450d-e054-00144ff88e88 |
Manufacturer | |
UNII | |
UPC Code |
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 |