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Mary Kay TimeWise Day Solution Sunscreen SPF 25
Mary Kay TimeWise Day Solution Sunscreen SPF 25 - 51531-2326-1 - (octinoxate, octisalate, zinc oxide, oxybenzone,)
Drug Information of Mary Kay TimeWise Day Solution Sunscreen SPF 25
| Product NDC: | 51531-2326 |
| Proprietary Name: | Mary Kay TimeWise Day Solution Sunscreen SPF 25 |
| Non Proprietary Name: | octinoxate, octisalate, zinc oxide, oxybenzone, |
| Active Ingredient(s): | 7.5; 5; 3; 3.88 g/100mL; g/100mL; g/100mL; g/100mL & nbsp; octinoxate, octisalate, zinc oxide, oxybenzone, |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mary Kay TimeWise Day Solution Sunscreen SPF 25
| Product NDC: | 51531-2326 |
| Labeler Name: | Mary Kay Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20051216 |
Package Information of Mary Kay TimeWise Day Solution Sunscreen SPF 25
| Package NDC: | 51531-2326-1 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (51531-2326-1) > 29 mL in 1 BOTTLE, PUMP |
NDC Information of Mary Kay TimeWise Day Solution Sunscreen SPF 25
| NDC Code | 51531-2326-1 |
| Proprietary Name | Mary Kay TimeWise Day Solution Sunscreen SPF 25 |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (51531-2326-1) > 29 mL in 1 BOTTLE, PUMP |
| Product NDC | 51531-2326 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | octinoxate, octisalate, zinc oxide, oxybenzone, |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20051216 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Mary Kay Inc. |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE; ZINC OXIDE |
| Strength Number | 7.5; 5; 3; 3.88 |
| Strength Unit | g/100mL; g/100mL; g/100mL; g/100mL |
| Pharmaceutical Classes |
