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Olay Complete All Day
Olay Complete All Day - 37000-238-75 - (Octinoxate, Octisalate, Octocrylene, and Zinc Oxide)
Drug Information of Olay Complete All Day
| Product NDC: | 37000-238 |
| Proprietary Name: | Olay Complete All Day |
| Non Proprietary Name: | Octinoxate, Octisalate, Octocrylene, and Zinc Oxide |
| Active Ingredient(s): | .075; .025; .025; .06 mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; Octinoxate, Octisalate, Octocrylene, and Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Olay Complete All Day
| Product NDC: | 37000-238 |
| Labeler Name: | Procter & Gamble Manufacturing Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120601 |
Package Information of Olay Complete All Day
| Package NDC: | 37000-238-75 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (37000-238-75) > 75 mL in 1 BOTTLE, PUMP |
NDC Information of Olay Complete All Day
| NDC Code | 37000-238-75 |
| Proprietary Name | Olay Complete All Day |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (37000-238-75) > 75 mL in 1 BOTTLE, PUMP |
| Product NDC | 37000-238 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Octisalate, Octocrylene, and Zinc Oxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120601 |
| 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 | mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
