| Product NDC: | 49893-500 |
| Proprietary Name: | Total Suncare Sunscreen SPF 70 |
| Non Proprietary Name: | AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE |
| Active Ingredient(s): | 3; 15; 5; 5; 5 mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49893-500 |
| Labeler Name: | Total Suncare LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20091208 |
| Package NDC: | 49893-500-01 |
| Package Description: | 177 mL in 1 BOTTLE, SPRAY (49893-500-01) |
| NDC Code | 49893-500-01 |
| Proprietary Name | Total Suncare Sunscreen SPF 70 |
| Package Description | 177 mL in 1 BOTTLE, SPRAY (49893-500-01) |
| Product NDC | 49893-500 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20091208 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Total Suncare LLC |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 3; 15; 5; 5; 5 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |