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La Roche Posay Laboratoire Dermatologique
La Roche Posay Laboratoire Dermatologique - 49967-907-01 - (Titanium dioxide and Zinc oxide)
Drug Information of La Roche Posay Laboratoire Dermatologique
| Product NDC: | 49967-907 |
| Proprietary Name: | La Roche Posay Laboratoire Dermatologique |
| Non Proprietary Name: | Titanium dioxide and Zinc oxide |
| Active Ingredient(s): | 60; 50 mg/mL; mg/mL & nbsp; Titanium dioxide and Zinc oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of La Roche Posay Laboratoire Dermatologique
| Product NDC: | 49967-907 |
| 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 Roche Posay Laboratoire Dermatologique
| Package NDC: | 49967-907-01 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (49967-907-01) > 50 mL in 1 BOTTLE, PLASTIC |
NDC Information of La Roche Posay Laboratoire Dermatologique
| NDC Code | 49967-907-01 |
| Proprietary Name | La Roche Posay Laboratoire Dermatologique |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (49967-907-01) > 50 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 49967-907 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Titanium dioxide and Zinc oxide |
| 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; ZINC OXIDE |
| Strength Number | 60; 50 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
