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: | 37000-239-25 |
Package Description: | 1 BOTTLE, PUMP in 1 CARTON (37000-239-25) > 75 mL in 1 BOTTLE, PUMP |
NDC Code | 37000-239-25 |
Proprietary Name | Olay Complete SPF 30 Defense Daily UV Moisturizer |
Package Description | 1 BOTTLE, PUMP in 1 CARTON (37000-239-25) > 75 mL in 1 BOTTLE, PUMP |
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 |