| Product NDC: | 37000-239 |
| Proprietary Name: | Olay Complete SPF 30 Defense Daily UV Moisturizer |
| Non Proprietary Name: | Octinoxate, Zinc Oxide, Octisalate, and Octocrylene |
| Active Ingredient(s): | .075; .025; .025; .06 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Octinoxate, Zinc Oxide, Octisalate, and Octocrylene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 37000-239 |
| 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: | 37000-239-06 |
| Package Description: | 1.77 mL in 1 POUCH (37000-239-06) |
| NDC Code | 37000-239-06 |
| Proprietary Name | Olay Complete SPF 30 Defense Daily UV Moisturizer |
| Package Description | 1.77 mL in 1 POUCH (37000-239-06) |
| Product NDC | 37000-239 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Zinc Oxide, Octisalate, 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 | OCTINOXATE; OCTISALATE; OCTOCRYLENE; ZINC OXIDE |
| Strength Number | .075; .025; .025; .06 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |