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Aloe Sunscreen
Aloe Sunscreen - 11697-199-04 - (Homosalate)
Drug Information of Aloe Sunscreen
| Product NDC: | 11697-199 |
| Proprietary Name: | Aloe Sunscreen |
| Non Proprietary Name: | Homosalate |
| Active Ingredient(s): | 3.54; 3.54; 1.18; 5.9; 3.922 mL/118mL; mL/118mL; mL/118mL; mL/118mL; mL/118mL & nbsp; Homosalate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aloe Sunscreen
| Product NDC: | 11697-199 |
| Labeler Name: | Aloe Vera of America, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110406 |
Package Information of Aloe Sunscreen
| Package NDC: | 11697-199-04 |
| Package Description: | 118 mL in 1 TUBE (11697-199-04) |
NDC Information of Aloe Sunscreen
| NDC Code | 11697-199-04 |
| Proprietary Name | Aloe Sunscreen |
| Package Description | 118 mL in 1 TUBE (11697-199-04) |
| Product NDC | 11697-199 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Homosalate |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110406 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Aloe Vera of America, Inc. |
| Substance Name | AVOBENZONE; ENSULIZOLE; HOMOSALATE; OCTISALATE; OCTOCRYLENE |
| Strength Number | 3.54; 3.54; 1.18; 5.9; 3.922 |
| Strength Unit | mL/118mL; mL/118mL; mL/118mL; mL/118mL; mL/118mL |
| Pharmaceutical Classes |
