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 |