| Product NDC: | 76157-222 |
| Proprietary Name: | Sun Protection Emulsion Face Broad Spectrum SPF 30 |
| Non Proprietary Name: | Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone |
| Active Ingredient(s): | 3; 10; 2.6; 2.4; 5 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL & nbsp; Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 76157-222 |
| Labeler Name: | La Prairie Group AG |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110214 |
| Package NDC: | 76157-222-02 |
| Package Description: | 1 TUBE in 1 CARTON (76157-222-02) > 125 mL in 1 TUBE (76157-222-01) |
| NDC Code | 76157-222-02 |
| Proprietary Name | Sun Protection Emulsion Face Broad Spectrum SPF 30 |
| Package Description | 1 TUBE in 1 CARTON (76157-222-02) > 125 mL in 1 TUBE (76157-222-01) |
| Product NDC | 76157-222 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110214 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | La Prairie Group AG |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 3; 10; 2.6; 2.4; 5 |
| Strength Unit | g/100mL; g/100mL; g/100mL; g/100mL; g/100mL |
| Pharmaceutical Classes |