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Neutrogena Pure and Free
Neutrogena Pure and Free - 10812-430-01 - (Titanium Dioxide and Zinc Oxide)
Drug Information of Neutrogena Pure and Free
| Product NDC: | 10812-430 |
| Proprietary Name: | Neutrogena Pure and Free |
| Non Proprietary Name: | Titanium Dioxide and Zinc Oxide |
| Active Ingredient(s): | 50; 30 mg/mL; mg/mL & nbsp; Titanium Dioxide and Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Neutrogena Pure and Free
| Product NDC: | 10812-430 |
| Labeler Name: | Neutrogena Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20121016 |
Package Information of Neutrogena Pure and Free
| Package NDC: | 10812-430-01 |
| Package Description: | 1 TUBE in 1 BLISTER PACK (10812-430-01) > 40 mL in 1 TUBE |
NDC Information of Neutrogena Pure and Free
| NDC Code | 10812-430-01 |
| Proprietary Name | Neutrogena Pure and Free |
| Package Description | 1 TUBE in 1 BLISTER PACK (10812-430-01) > 40 mL in 1 TUBE |
| Product NDC | 10812-430 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Titanium Dioxide and Zinc Oxide |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20121016 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Neutrogena Corporation |
| Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 50; 30 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
