Product NDC: | 37000-770 |
Proprietary Name: | Olay Anti-Wrinkle 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) |
Product NDC: | 37000-770 |
Labeler Name: | The Procter & Gamble Manufacturing Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20091101 |
Package NDC: | 37000-770-11 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (37000-770-11) > 118 mL in 1 BOTTLE, PLASTIC |
NDC Code | 37000-770-11 |
Proprietary Name | Olay Anti-Wrinkle Mature Skin |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (37000-770-11) > 118 mL in 1 BOTTLE, PLASTIC |
Product NDC | 37000-770 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate and Zinc Oxide |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20091101 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | The Procter & Gamble Manufacturing Company |
Substance Name | OCTINOXATE; ZINC OXIDE |
Strength Number | 58.8; 29.4 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |