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Neutrogena Pure and free Baby Sunblock
Neutrogena Pure and free Baby Sunblock - 10812-322-01 - (Titanium Dioxide and Zinc Oxide)
Drug Information of Neutrogena Pure and free Baby Sunblock
| Product NDC: | 10812-322 |
| Proprietary Name: | Neutrogena Pure and free Baby Sunblock |
| Non Proprietary Name: | Titanium Dioxide and Zinc Oxide |
| Active Ingredient(s): | 49; 47 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 Neutrogena Pure and free Baby Sunblock
| Product NDC: | 10812-322 |
| Labeler Name: | Neutrogena Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20101201 |
Package Information of Neutrogena Pure and free Baby Sunblock
| Package NDC: | 10812-322-01 |
| Package Description: | 88 mL in 1 TUBE (10812-322-01) |
NDC Information of Neutrogena Pure and free Baby Sunblock
| NDC Code | 10812-322-01 |
| Proprietary Name | Neutrogena Pure and free Baby Sunblock |
| Package Description | 88 mL in 1 TUBE (10812-322-01) |
| Product NDC | 10812-322 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Titanium Dioxide and Zinc Oxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20101201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Neutrogena Corporation |
| Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 49; 47 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
