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Sunleya Age Minimizing Sun Care
Sunleya Age Minimizing Sun Care - 66097-002-50 - (AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE)
Drug Information of Sunleya Age Minimizing Sun Care
| Product NDC: | 66097-002 |
| Proprietary Name: | Sunleya Age Minimizing Sun Care |
| Non Proprietary Name: | AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE |
| Active Ingredient(s): | 30; 50; 50; 40 mg/g; mg/g; mg/g; mg/g & nbsp; AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sunleya Age Minimizing Sun Care
| Product NDC: | 66097-002 |
| 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 Information of Sunleya Age Minimizing Sun Care
| Package NDC: | 66097-002-50 |
| Package Description: | 1 BOTTLE in 1 BOX (66097-002-50) > 50.3 g in 1 BOTTLE |
NDC Information of Sunleya Age Minimizing Sun Care
| NDC Code | 66097-002-50 |
| Proprietary Name | Sunleya Age Minimizing Sun Care |
| Package Description | 1 BOTTLE in 1 BOX (66097-002-50) > 50.3 g in 1 BOTTLE |
| Product NDC | 66097-002 |
| 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/g; mg/g; mg/g; mg/g |
| Pharmaceutical Classes |
