Home
>
National Drug Code (NDC)
>
La Roche Posay Laboratoire Dermatologique Anthelios 60 Ultra Light Sunscreen Fluid
La Roche Posay Laboratoire Dermatologique Anthelios 60 Ultra Light Sunscreen Fluid - 49967-993-01 - (Avobenzone, Homosalate, Octisalate, Octocrylene and Oxybenzone)
Drug Information of La Roche Posay Laboratoire Dermatologique Anthelios 60 Ultra Light Sunscreen Fluid
| Product NDC: | 49967-993 |
| Proprietary Name: | La Roche Posay Laboratoire Dermatologique Anthelios 60 Ultra Light Sunscreen Fluid |
| Non Proprietary Name: | Avobenzone, Homosalate, Octisalate, Octocrylene and Oxybenzone |
| Active Ingredient(s): | 30; 107.2; 32.1; 60; 38.6 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Avobenzone, Homosalate, Octisalate, Octocrylene and Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of La Roche Posay Laboratoire Dermatologique Anthelios 60 Ultra Light Sunscreen Fluid
| Product NDC: | 49967-993 |
| 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: | 20130301 |
Package Information of La Roche Posay Laboratoire Dermatologique Anthelios 60 Ultra Light Sunscreen Fluid
| Package NDC: | 49967-993-01 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (49967-993-01) > 50 mL in 1 BOTTLE, PLASTIC |
NDC Information of La Roche Posay Laboratoire Dermatologique Anthelios 60 Ultra Light Sunscreen Fluid
| NDC Code | 49967-993-01 |
| Proprietary Name | La Roche Posay Laboratoire Dermatologique Anthelios 60 Ultra Light Sunscreen Fluid |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (49967-993-01) > 50 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 49967-993 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Homosalate, Octisalate, Octocrylene and Oxybenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20130301 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | L'Oreal USA Products Inc |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 30; 107.2; 32.1; 60; 38.6 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
