| Product NDC: | 58232-0716 |
| Proprietary Name: | Aveeno Daily Moisturizing |
| Non Proprietary Name: | Avobenzone, Octisalate, Octocrylene, and Oxybenzone |
| Active Ingredient(s): | 30; 50; 17; 30 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Avobenzone, Octisalate, Octocrylene, and Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 58232-0716 |
| 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 FINAL |
| Start Marketing Date: | 20110812 |
| Package NDC: | 58232-0716-1 |
| Package Description: | 240 mL in 1 TUBE (58232-0716-1) |
| NDC Code | 58232-0716-1 |
| Proprietary Name | Aveeno Daily Moisturizing |
| Package Description | 240 mL in 1 TUBE (58232-0716-1) |
| Product NDC | 58232-0716 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Octisalate, Octocrylene, and Oxybenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110812 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Substance Name | AVOBENZONE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 30; 50; 17; 30 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |