Product NDC: | 49893-300 |
Proprietary Name: | Total Suncare Sunscreen SPF 50 |
Non Proprietary Name: | AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE |
Active Ingredient(s): | 3; 10; 3; 3; 4 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: | 49893-300 |
Labeler Name: | Total Suncare LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20091125 |
Package NDC: | 49893-300-01 |
Package Description: | 177 mL in 1 BOTTLE, SPRAY (49893-300-01) |
NDC Code | 49893-300-01 |
Proprietary Name | Total Suncare Sunscreen SPF 50 |
Package Description | 177 mL in 1 BOTTLE, SPRAY (49893-300-01) |
Product NDC | 49893-300 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE |
Dosage Form Name | SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 20091125 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Total Suncare LLC |
Substance Name | AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE |
Strength Number | 3; 10; 3; 3; 4 |
Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL |
Pharmaceutical Classes |