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Timewise Day Solution sunscreen SPF 35
Timewise Day Solution sunscreen SPF 35 - 51531-8363-0 - (Homosalate,Octisalate,Oxybenzone,Octocrylene,Avobenzone)
Drug Information of Timewise Day Solution sunscreen SPF 35
| Product NDC: | 51531-8363 |
| Proprietary Name: | Timewise Day Solution sunscreen SPF 35 |
| Non Proprietary Name: | Homosalate,Octisalate,Oxybenzone,Octocrylene,Avobenzone |
| Active Ingredient(s): | .58; 2.9; 1.45; .58; 1.16 mL/29mL; mL/29mL; mL/29mL; mL/29mL; mL/29mL & nbsp; Homosalate,Octisalate,Oxybenzone,Octocrylene,Avobenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Timewise Day Solution sunscreen SPF 35
| Product NDC: | 51531-8363 |
| Labeler Name: | Mary Kay Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120301 |
Package Information of Timewise Day Solution sunscreen SPF 35
| Package NDC: | 51531-8363-0 |
| Package Description: | 29 mL in 1 BOTTLE, DISPENSING (51531-8363-0) |
NDC Information of Timewise Day Solution sunscreen SPF 35
| NDC Code | 51531-8363-0 |
| Proprietary Name | Timewise Day Solution sunscreen SPF 35 |
| Package Description | 29 mL in 1 BOTTLE, DISPENSING (51531-8363-0) |
| Product NDC | 51531-8363 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Homosalate,Octisalate,Oxybenzone,Octocrylene,Avobenzone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120301 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Mary Kay Inc. |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | .58; 2.9; 1.45; .58; 1.16 |
| Strength Unit | mL/29mL; mL/29mL; mL/29mL; mL/29mL; mL/29mL |
| Pharmaceutical Classes |
