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Aveeno
Aveeno - 58232-0512-2 - (Homosalate, Octinoxate, Octisalate and Titanium Dioxide)
Drug Information of Aveeno
| Product NDC: | 58232-0512 |
| Proprietary Name: | Aveeno |
| Non Proprietary Name: | Homosalate, Octinoxate, Octisalate and Titanium Dioxide |
| Active Ingredient(s): | 51.3; 76.9; 51.3; 24.6 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Homosalate, Octinoxate, Octisalate and Titanium Dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aveeno
| Product NDC: | 58232-0512 |
| Labeler Name: | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090825 |
Package Information of Aveeno
| Package NDC: | 58232-0512-2 |
| Package Description: | 10 mL in 1 TUBE (58232-0512-2) |
NDC Information of Aveeno
| NDC Code | 58232-0512-2 |
| Proprietary Name | Aveeno |
| Package Description | 10 mL in 1 TUBE (58232-0512-2) |
| Product NDC | 58232-0512 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Homosalate, Octinoxate, Octisalate and Titanium Dioxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20090825 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Substance Name | HOMOSALATE; OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE |
| Strength Number | 51.3; 76.9; 51.3; 24.6 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
