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 |