Product NDC: | 37000-244 |
Proprietary Name: | Olay Complete All Day UV Moisturizer |
Non Proprietary Name: | Octisalate, Avobenzone, Homosalate, and Octocrylene |
Active Ingredient(s): | 29.4; 29.4; 49; 25.48 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Octisalate, Avobenzone, Homosalate, and Octocrylene |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 37000-244 |
Labeler Name: | Procter & Gamble Manufacturing Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090701 |
Package NDC: | 37000-244-60 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (37000-244-60) > 177 mL in 1 BOTTLE, PLASTIC |
NDC Code | 37000-244-60 |
Proprietary Name | Olay Complete All Day UV Moisturizer |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (37000-244-60) > 177 mL in 1 BOTTLE, PLASTIC |
Product NDC | 37000-244 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octisalate, Avobenzone, Homosalate, and Octocrylene |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20090701 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Procter & Gamble Manufacturing Company |
Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE |
Strength Number | 29.4; 29.4; 49; 25.48 |
Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |