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Olay Complete All Day
Olay Complete All Day - 37000-752-17 - (Avobenzone, Homosalate, Octisalate, and Octocrylene)
Drug Information of Olay Complete All Day
| Product NDC: | 37000-752 |
| Proprietary Name: | Olay Complete All Day |
| Non Proprietary Name: | Avobenzone, Homosalate, Octisalate, and Octocrylene |
| Active Ingredient(s): | .03; .05; .05; .026 mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; Avobenzone, Homosalate, Octisalate, and Octocrylene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Olay Complete All Day
| Product NDC: | 37000-752 |
| Labeler Name: | Procter & Gamble Manufacturing Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120501 |
Package Information of Olay Complete All Day
| Package NDC: | 37000-752-17 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (37000-752-17) > 177 mL in 1 BOTTLE, PLASTIC |
NDC Information of Olay Complete All Day
| NDC Code | 37000-752-17 |
| Proprietary Name | Olay Complete All Day |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (37000-752-17) > 177 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 37000-752 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Homosalate, Octisalate, and Octocrylene |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120501 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Procter & Gamble Manufacturing Company |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE |
| Strength Number | .03; .05; .05; .026 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
