Product NDC: | 76169-101 |
Proprietary Name: | Renewing Antioxidant Treatment SPF 6 |
Non Proprietary Name: | Octyl Methoxycinnamate, Avobenzone |
Active Ingredient(s): | 1.7; 6 g/100g; g/100g & nbsp; Octyl Methoxycinnamate, Avobenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76169-101 |
Labeler Name: | GNLD International |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110422 |
Package NDC: | 76169-101-02 |
Package Description: | 1 JAR in 1 BOX (76169-101-02) > 50 g in 1 JAR (76169-101-01) |
NDC Code | 76169-101-02 |
Proprietary Name | Renewing Antioxidant Treatment SPF 6 |
Package Description | 1 JAR in 1 BOX (76169-101-02) > 50 g in 1 JAR (76169-101-01) |
Product NDC | 76169-101 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octyl Methoxycinnamate, Avobenzone |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20110422 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | GNLD International |
Substance Name | AVOBENZONE; OCTINOXATE |
Strength Number | 1.7; 6 |
Strength Unit | g/100g; g/100g |
Pharmaceutical Classes |