| 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: | 76157-738-11 |
| Package Description: | .005 g in 1 CANISTER (76157-738-11) |
| NDC Code | 76157-738-11 |
| Proprietary Name | Ultra Protection stick SPF 40 |
| Package Description | .005 g in 1 CANISTER (76157-738-11) |
| 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 |