| NDC Code | 49967-222-01 |
|---|
| Package Description | 1 BOTTLE in 1 CARTON (49967-222-01) > 50 mL in 1 BOTTLE |
|---|
| Product NDC | 49967-222 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | La Roche Posay Laboratoire Dermatologique Anthelios 45 Ultra Light Sunscreen Fluid Water Resistant 40 |
|---|
| Non-Proprietary Name | Avobenzone, Homosalate, Octisalate, Octocrylene And Oxybenzone |
|---|
| Dosage Form | LOTION |
|---|
| Usage | TOPICAL |
|---|
| Start Marketing Date | 20100401 |
|---|
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
|---|
| Application Number | part352 |
|---|
| Manufacturer | L'Oreal USA Products Inc |
|---|
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
|---|
| Strength | 30; 100; 50; 50; 60 |
|---|
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL; mg/mL |
|---|