Product NDC: | 66097-004 |
Proprietary Name: | Super Creme Solaire Corps Body SunCare |
Non Proprietary Name: | AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE |
Active Ingredient(s): | 30; 50; 50; 40 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 66097-004 |
Labeler Name: | C.F.E.B. Sisley |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130121 |
Package NDC: | 66097-004-00 |
Package Description: | 1 TUBE in 1 BOX (66097-004-00) > 200 mL in 1 TUBE |
NDC Code | 66097-004-00 |
Proprietary Name | Super Creme Solaire Corps Body SunCare |
Package Description | 1 TUBE in 1 BOX (66097-004-00) > 200 mL in 1 TUBE |
Product NDC | 66097-004 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20130121 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | C.F.E.B. Sisley |
Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE |
Strength Number | 30; 50; 50; 40 |
Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |