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La RochePosay Laboratoire Dermatologique
La RochePosay Laboratoire Dermatologique - 49967-090-01 - (Titanium dioxide)
Drug Information of La RochePosay Laboratoire Dermatologique
| Product NDC: | 49967-090 |
| Proprietary Name: | La RochePosay Laboratoire Dermatologique |
| Non Proprietary Name: | Titanium dioxide |
| Active Ingredient(s): | 5.5 mL/50mL & nbsp; Titanium dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of La RochePosay Laboratoire Dermatologique
| Product NDC: | 49967-090 |
| 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: | 20110701 |
Package Information of La RochePosay Laboratoire Dermatologique
| Package NDC: | 49967-090-01 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (49967-090-01) > 50 mL in 1 BOTTLE, PLASTIC |
NDC Information of La RochePosay Laboratoire Dermatologique
| NDC Code | 49967-090-01 |
| Proprietary Name | La RochePosay Laboratoire Dermatologique |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (49967-090-01) > 50 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 49967-090 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Titanium dioxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110701 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | L'Oreal USA Products Inc |
| Substance Name | TITANIUM DIOXIDE |
| Strength Number | 5.5 |
| Strength Unit | mL/50mL |
| Pharmaceutical Classes |
