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Anti-Wrinkle SunScreen
Anti-Wrinkle SunScreen - 76157-411-02 - (Avobenzone, Octinoxate, Octisalate, Octocrylene, Oxybenzone)
Drug Information of Anti-Wrinkle SunScreen
| Product NDC: | 76157-411 |
| Proprietary Name: | Anti-Wrinkle SunScreen |
| Non Proprietary Name: | Avobenzone, Octinoxate, Octisalate, Octocrylene, Oxybenzone |
| Active Ingredient(s): | 3; 7.5; 2.6; 2.4; 5 mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; Avobenzone, Octinoxate, Octisalate, Octocrylene, Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Anti-Wrinkle SunScreen
| Product NDC: | 76157-411 |
| Labeler Name: | La Prairie Group AG |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090101 |
Package Information of Anti-Wrinkle SunScreen
| Package NDC: | 76157-411-02 |
| Package Description: | 1 JAR in 1 CARTON (76157-411-02) > 50 mL in 1 JAR (76157-411-01) |
NDC Information of Anti-Wrinkle SunScreen
| NDC Code | 76157-411-02 |
| Proprietary Name | Anti-Wrinkle SunScreen |
| Package Description | 1 JAR in 1 CARTON (76157-411-02) > 50 mL in 1 JAR (76157-411-01) |
| Product NDC | 76157-411 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Octinoxate, Octisalate, Octocrylene, Oxybenzone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20090101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | La Prairie Group AG |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 3; 7.5; 2.6; 2.4; 5 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
