Aloe Sunscreen is a Topical Spray in the Human Otc Drug category. It is labeled and distributed by Aloe Vera Of America, Inc.. The primary component is Homosalate; Octisalate; Ensulizole; Avobenzone; Octocrylene.
Product ID | 11697-319_50c98089-b653-428f-bb12-5cd65b50b9a8 |
NDC | 11697-319 |
Product Type | Human Otc Drug |
Proprietary Name | Aloe Sunscreen |
Generic Name | Homosalate, Octisalate, Avobenzone, Ensulizole Anf Octocrylene |
Dosage Form | Spray |
Route of Administration | TOPICAL |
Marketing Start Date | 2010-08-16 |
Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
Application Number | part352 |
Labeler Name | Aloe Vera of America, Inc. |
Substance Name | HOMOSALATE; OCTISALATE; ENSULIZOLE; AVOBENZONE; OCTOCRYLENE |
Active Ingredient Strength | 10 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL |
NDC Exclude Flag | E |
Listing Certified Through | 2017-12-31 |
Marketing Start Date | 2010-08-16 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-01-30 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-08-16 |
Marketing End Date | 2015-01-30 |
Ingredient | Strength |
---|---|
HOMOSALATE | 10 g/100mL |
SPL SET ID: | d1fc6718-8611-44b5-b312-8cf4866cb46b |
Manufacturer | |
UNII |
NDC | Brand Name | Generic Name |
---|---|---|
11697-199 | Aloe Sunscreen | Homosalate, Octisalate, Avobenzone, Ensulizole and Octocrylene |
11697-319 | Aloe Sunscreen | Homosalate, Octisalate, Avobenzone, Ensulizole anf Octocrylene |