Home
>
National Drug Code (NDC)
>
Olay Age Defying Protective Renewal
Olay Age Defying Protective Renewal - 37000-250-01 - (Octinoxate and Zinc Oxide)
Drug Information of Olay Age Defying Protective Renewal
| Product NDC: | 37000-250 |
| Proprietary Name: | Olay Age Defying Protective Renewal |
| Non Proprietary Name: | Octinoxate and Zinc Oxide |
| Active Ingredient(s): | 60; 30 mg/mL; mg/mL & nbsp; Octinoxate and Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Olay Age Defying Protective Renewal
| Product NDC: | 37000-250 |
| Labeler Name: | Procter & Gamble Manufacturing Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19981201 |
Package Information of Olay Age Defying Protective Renewal
| Package NDC: | 37000-250-01 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (37000-250-01) > 118 mL in 1 BOTTLE, PLASTIC |
NDC Information of Olay Age Defying Protective Renewal
| NDC Code | 37000-250-01 |
| Proprietary Name | Olay Age Defying Protective Renewal |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (37000-250-01) > 118 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 37000-250 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate and Zinc Oxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 19981201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Procter & Gamble Manufacturing Company |
| Substance Name | OCTINOXATE; ZINC OXIDE |
| Strength Number | 60; 30 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
