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Aloe Sunscreen
Aloe Sunscreen - 11697-319-06 - (Homosalate)
Drug Information of Aloe Sunscreen
| Product NDC: | 11697-319 |
| Proprietary Name: | Aloe Sunscreen |
| Non Proprietary Name: | Homosalate |
| Active Ingredient(s): | 5.34; 7.12; 17.8; 8.9; 4.9662 mL/178mL; mL/178mL; mL/178mL; mL/178mL; mL/178mL & nbsp; Homosalate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aloe Sunscreen
| Product NDC: | 11697-319 |
| 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: | 20100816 |
Package Information of Aloe Sunscreen
| Package NDC: | 11697-319-06 |
| Package Description: | 178 mL in 1 BOTTLE, SPRAY (11697-319-06) |
NDC Information of Aloe Sunscreen
| NDC Code | 11697-319-06 |
| Proprietary Name | Aloe Sunscreen |
| Package Description | 178 mL in 1 BOTTLE, SPRAY (11697-319-06) |
| Product NDC | 11697-319 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Homosalate |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20100816 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Aloe Vera of America, Inc. |
| Substance Name | AVOBENZONE; ENSULIZOLE; HOMOSALATE; OCTISALATE; OCTOCRYLENE |
| Strength Number | 5.34; 7.12; 17.8; 8.9; 4.9662 |
| Strength Unit | mL/178mL; mL/178mL; mL/178mL; mL/178mL; mL/178mL |
| Pharmaceutical Classes |
