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 |