| Product NDC: | 53675-150 |
| Proprietary Name: | Aruba Aloe Very Water Resistant Sunscreen |
| Non Proprietary Name: | HOMOSALATE, OCTINOXATE, PADIMATE O , OXYBENZONE |
| Active Ingredient(s): | 8; 7; 3; 4.2 mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; HOMOSALATE, OCTINOXATE, PADIMATE O , OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 53675-150 |
| Labeler Name: | Aruba Aloe Balm, NV |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110605 |
| Package NDC: | 53675-150-02 |
| Package Description: | 65 mL in 1 BOTTLE (53675-150-02) |
| NDC Code | 53675-150-02 |
| Proprietary Name | Aruba Aloe Very Water Resistant Sunscreen |
| Package Description | 65 mL in 1 BOTTLE (53675-150-02) |
| Product NDC | 53675-150 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HOMOSALATE, OCTINOXATE, PADIMATE O , OXYBENZONE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110605 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Aruba Aloe Balm, NV |
| Substance Name | HOMOSALATE; OCTINOXATE; OXYBENZONE; PADIMATE O |
| Strength Number | 8; 7; 3; 4.2 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |