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Anti-Aging Emulsion
Anti-Aging Emulsion - 76157-274-02 - (Avobenzone, Octinoxate, Octisalate, Oxybenzone)
Drug Information of Anti-Aging Emulsion
| Product NDC: | 76157-274 |
| Proprietary Name: | Anti-Aging Emulsion |
| Non Proprietary Name: | Avobenzone, Octinoxate, Octisalate, Oxybenzone |
| Active Ingredient(s): | 2.8; 7.5; 5; 4 mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; Avobenzone, Octinoxate, Octisalate, Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Anti-Aging Emulsion
| Product NDC: | 76157-274 |
| Labeler Name: | La Prairie Group AG |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110513 |
Package Information of Anti-Aging Emulsion
| Package NDC: | 76157-274-02 |
| Package Description: | 1 JAR in 1 BOX (76157-274-02) > 50 mL in 1 JAR (76157-274-01) |
NDC Information of Anti-Aging Emulsion
| NDC Code | 76157-274-02 |
| Proprietary Name | Anti-Aging Emulsion |
| Package Description | 1 JAR in 1 BOX (76157-274-02) > 50 mL in 1 JAR (76157-274-01) |
| Product NDC | 76157-274 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Octinoxate, Octisalate, Oxybenzone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110513 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | La Prairie Group AG |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 2.8; 7.5; 5; 4 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
