Product NDC: | 49967-095 |
Proprietary Name: | La Roche Posay Laboratoire Dermatologique |
Non Proprietary Name: | Avobenzone Homosalate Octisalate Octocrylene Oxybenzone |
Active Ingredient(s): | 1.2; 4; 2; 2; 2.4 mL/40mL; mL/40mL; mL/40mL; mL/40mL; mL/40mL & nbsp; Avobenzone Homosalate Octisalate Octocrylene Oxybenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49967-095 |
Labeler Name: | L'Oreal USA Products Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120405 |
Package NDC: | 49967-095-01 |
Package Description: | 1 TUBE in 1 CARTON (49967-095-01) > 40 mL in 1 TUBE |
NDC Code | 49967-095-01 |
Proprietary Name | La Roche Posay Laboratoire Dermatologique |
Package Description | 1 TUBE in 1 CARTON (49967-095-01) > 40 mL in 1 TUBE |
Product NDC | 49967-095 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Avobenzone Homosalate Octisalate Octocrylene Oxybenzone |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20120405 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | L'Oreal USA Products Inc |
Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
Strength Number | 1.2; 4; 2; 2; 2.4 |
Strength Unit | mL/40mL; mL/40mL; mL/40mL; mL/40mL; mL/40mL |
Pharmaceutical Classes |