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Olay Age Defying Mature Skin
Olay Age Defying Mature Skin - 37000-231-12 - (Octinoxate and Zinc Oxide)
Drug Information of Olay Age Defying Mature Skin
| Product NDC: | 37000-231 |
| Proprietary Name: | Olay Age Defying Mature Skin |
| Non Proprietary Name: | Octinoxate and Zinc Oxide |
| Active Ingredient(s): | 58.8; 29.4 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 Mature Skin
| Product NDC: | 37000-231 |
| Labeler Name: | Procter & Gamble Manufacturing Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120401 |
Package Information of Olay Age Defying Mature Skin
| Package NDC: | 37000-231-12 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (37000-231-12) > 120 mL in 1 BOTTLE, PLASTIC |
NDC Information of Olay Age Defying Mature Skin
| NDC Code | 37000-231-12 |
| Proprietary Name | Olay Age Defying Mature Skin |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (37000-231-12) > 120 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 37000-231 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate and Zinc Oxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120401 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Procter & Gamble Manufacturing Company |
| Substance Name | OCTINOXATE; ZINC OXIDE |
| Strength Number | 58.8; 29.4 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
