| Product NDC: | 37000-279 |
| Proprietary Name: | Olay Total Effects |
| Non Proprietary Name: | Octisalate, Avobenzone, Ensulizole, and Octocrylene |
| Active Ingredient(s): | 20; 10; 40; 10 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Octisalate, Avobenzone, Ensulizole, and Octocrylene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 37000-279 |
| Labeler Name: | Procter & Gamble Manufacturing Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20040101 |
| Package NDC: | 37000-279-17 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (37000-279-17) > 50 mL in 1 BOTTLE, PUMP |
| NDC Code | 37000-279-17 |
| Proprietary Name | Olay Total Effects |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (37000-279-17) > 50 mL in 1 BOTTLE, PUMP |
| Product NDC | 37000-279 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octisalate, Avobenzone, Ensulizole, and Octocrylene |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20040101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Procter & Gamble Manufacturing Company |
| Substance Name | AVOBENZONE; ENSULIZOLE; OCTISALATE; OCTOCRYLENE |
| Strength Number | 20; 10; 40; 10 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |