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: | 58232-0716-2 |
Package Description: | 354 mL in 1 BOTTLE, PUMP (58232-0716-2) |
NDC Code | 58232-0716-2 |
Proprietary Name | Aveeno Daily Moisturizing |
Package Description | 354 mL in 1 BOTTLE, PUMP (58232-0716-2) |
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 |