| Product NDC: | 76157-738 | 
| Proprietary Name: | Ultra Protection stick SPF 40 | 
| Non Proprietary Name: | Avobenzone, Homosalate, Octisalate, Oxybenzone | 
| Active Ingredient(s): | 3; 7; 5; 2 g/100g; g/100g; g/100g; g/100g & nbsp; Avobenzone, Homosalate, Octisalate, Oxybenzone | 
| Administration Route(s): | TOPICAL | 
| Dosage Form(s): | STICK | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 76157-738 | 
| Labeler Name: | La Prairie Group AG | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part352 | 
| Marketing Category: | OTC MONOGRAPH FINAL | 
| Start Marketing Date: | 20110214 | 
| Package NDC: | 76157-738-02 | 
| Package Description: | 1 BOTTLE in 1 BOX (76157-738-02) > 10 g in 1 BOTTLE (76157-738-01) | 
| NDC Code | 76157-738-02 | 
| Proprietary Name | Ultra Protection stick SPF 40 | 
| Package Description | 1 BOTTLE in 1 BOX (76157-738-02) > 10 g in 1 BOTTLE (76157-738-01) | 
| Product NDC | 76157-738 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Avobenzone, Homosalate, Octisalate, Oxybenzone | 
| Dosage Form Name | STICK | 
| Route Name | TOPICAL | 
| Start Marketing Date | 20110214 | 
| Marketing Category Name | OTC MONOGRAPH FINAL | 
| Labeler Name | La Prairie Group AG | 
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OXYBENZONE | 
| Strength Number | 3; 7; 5; 2 | 
| Strength Unit | g/100g; g/100g; g/100g; g/100g | 
| Pharmaceutical Classes |