Product NDC: | 62839-1332 |
Proprietary Name: | Sunright Broad Spectrum SPF 30 |
Non Proprietary Name: | Avobenzone, Octinoxate, Octisalate, and Oxybenzone |
Active Ingredient(s): | 30; 75; 50; 50 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Avobenzone, Octinoxate, Octisalate, and Oxybenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 62839-1332 |
Labeler Name: | NSE Products, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100901 |
Package NDC: | 62839-1332-1 |
Package Description: | 1 TUBE in 1 CARTON (62839-1332-1) > 100 mL in 1 TUBE |
NDC Code | 62839-1332-1 |
Proprietary Name | Sunright Broad Spectrum SPF 30 |
Package Description | 1 TUBE in 1 CARTON (62839-1332-1) > 100 mL in 1 TUBE |
Product NDC | 62839-1332 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Avobenzone, Octinoxate, Octisalate, and Oxybenzone |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20100901 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | NSE Products, Inc. |
Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE |
Strength Number | 30; 75; 50; 50 |
Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |