| Product NDC: | 53675-158 |
| Proprietary Name: | Aruba Aloe Very Water Resistant Sunscreen |
| Non Proprietary Name: | OCTOCRYLENE, OCTINOXATE, OXYBENZONE, HOMOSALATE, OCTYL SALICYLATE, AVOBENZONE |
| Active Ingredient(s): | 30; 50; 75; 50; 100; 60 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL; mg/mL & nbsp; OCTOCRYLENE, OCTINOXATE, OXYBENZONE, HOMOSALATE, OCTYL SALICYLATE, AVOBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 53675-158 |
| Labeler Name: | Aruba Aloe Balm NV |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130226 |
| Package NDC: | 53675-158-08 |
| Package Description: | 251 mL in 1 BOTTLE (53675-158-08) |
| NDC Code | 53675-158-08 |
| Proprietary Name | Aruba Aloe Very Water Resistant Sunscreen |
| Package Description | 251 mL in 1 BOTTLE (53675-158-08) |
| Product NDC | 53675-158 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTOCRYLENE, OCTINOXATE, OXYBENZONE, HOMOSALATE, OCTYL SALICYLATE, AVOBENZONE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20130226 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Aruba Aloe Balm NV |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 30; 50; 75; 50; 100; 60 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |