| Product NDC: | 76157-514 | 
| Proprietary Name: | Sun Protection Body Sunscreen Broad Spectrum SPF 30 | 
| Non Proprietary Name: | Avobenzone, Homosalate, Octisalate, Oxybenzone | 
| Active Ingredient(s): | 3; 7; 5; 5 g/100mL; g/100mL; g/100mL; g/100mL & nbsp; Avobenzone, Homosalate, Octisalate, Oxybenzone | 
| Administration Route(s): | TOPICAL | 
| Dosage Form(s): | LOTION | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 76157-514 | 
| Labeler Name: | La Prairie Group AG | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part352 | 
| Marketing Category: | OTC MONOGRAPH NOT FINAL | 
| Start Marketing Date: | 20130405 | 
| Package NDC: | 76157-514-02 | 
| Package Description: | 1 TUBE in 1 CARTON (76157-514-02) > 180 mL in 1 TUBE (76157-514-01) | 
| NDC Code | 76157-514-02 | 
| Proprietary Name | Sun Protection Body Sunscreen Broad Spectrum SPF 30 | 
| Package Description | 1 TUBE in 1 CARTON (76157-514-02) > 180 mL in 1 TUBE (76157-514-01) | 
| Product NDC | 76157-514 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Avobenzone, Homosalate, Octisalate, Oxybenzone | 
| Dosage Form Name | LOTION | 
| Route Name | TOPICAL | 
| Start Marketing Date | 20130405 | 
| Marketing Category Name | OTC MONOGRAPH NOT FINAL | 
| Labeler Name | La Prairie Group AG | 
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OXYBENZONE | 
| Strength Number | 3; 7; 5; 5 | 
| Strength Unit | g/100mL; g/100mL; g/100mL; g/100mL | 
| Pharmaceutical Classes |