Product NDC: | 53675-157 |
Proprietary Name: | Aruba Aloe Very Water Resistant Sunscreen |
Non Proprietary Name: | OCTINOXATE, OXYBENZONE |
Active Ingredient(s): | 7; 2 mL/100mL; mL/100mL & nbsp; OCTINOXATE, OXYBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 53675-157 |
Labeler Name: | Aruba Aloe Balm, NV |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110708 |
Package NDC: | 53675-157-06 |
Package Description: | 177 mL in 1 BOTTLE (53675-157-06) |
NDC Code | 53675-157-06 |
Proprietary Name | Aruba Aloe Very Water Resistant Sunscreen |
Package Description | 177 mL in 1 BOTTLE (53675-157-06) |
Product NDC | 53675-157 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, OXYBENZONE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20110708 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Aruba Aloe Balm, NV |
Substance Name | OCTINOXATE; OXYBENZONE |
Strength Number | 7; 2 |
Strength Unit | mL/100mL; mL/100mL |
Pharmaceutical Classes |