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Mary Kay TimeWise Day Solution SPF 35
Mary Kay TimeWise Day Solution SPF 35 - 51531-8360-1 - (avobenzone, homosalate, octisalate, octocrylene, oxybenzone)
Drug Information of Mary Kay TimeWise Day Solution SPF 35
| Product NDC: | 51531-8360 |
| Proprietary Name: | Mary Kay TimeWise Day Solution SPF 35 |
| Non Proprietary Name: | avobenzone, homosalate, octisalate, octocrylene, oxybenzone |
| Active Ingredient(s): | 2; 10; 5; 2; 4 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL & nbsp; avobenzone, homosalate, octisalate, octocrylene, oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mary Kay TimeWise Day Solution SPF 35
| Product NDC: | 51531-8360 |
| Labeler Name: | Mary Kay Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120301 |
Package Information of Mary Kay TimeWise Day Solution SPF 35
| Package NDC: | 51531-8360-1 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (51531-8360-1) > 29 mL in 1 BOTTLE, PUMP |
NDC Information of Mary Kay TimeWise Day Solution SPF 35
| NDC Code | 51531-8360-1 |
| Proprietary Name | Mary Kay TimeWise Day Solution SPF 35 |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (51531-8360-1) > 29 mL in 1 BOTTLE, PUMP |
| Product NDC | 51531-8360 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | avobenzone, homosalate, octisalate, octocrylene, oxybenzone |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120301 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Mary Kay Inc. |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 2; 10; 5; 2; 4 |
| Strength Unit | g/100mL; g/100mL; g/100mL; g/100mL; g/100mL |
| Pharmaceutical Classes |
