| Product NDC: | 37000-201 |
| Proprietary Name: | Olay Age Defying Anti-Wrinkle Daily |
| Non Proprietary Name: | Avobenzone, Homosalate, Octisalate, and Octocrylene |
| Active Ingredient(s): | 29.4; 49; 49; 25.4 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Avobenzone, Homosalate, Octisalate, and Octocrylene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 37000-201 |
| Labeler Name: | Procter & Gamble Manufacturing Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110601 |
| Package NDC: | 37000-201-34 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (37000-201-34) > 100 mL in 1 BOTTLE, PLASTIC |
| NDC Code | 37000-201-34 |
| Proprietary Name | Olay Age Defying Anti-Wrinkle Daily |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (37000-201-34) > 100 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 37000-201 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Homosalate, Octisalate, and Octocrylene |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110601 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Procter & Gamble Manufacturing Company |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE |
| Strength Number | 29.4; 49; 49; 25.4 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |