Product NDC: | 51531-4250 |
Proprietary Name: | Mary Kay Suncare Sunscreen Broad Spectrum SPF 50 |
Non Proprietary Name: | avobenzone, homosalate, octisalate, octocrylene, oxybenzone |
Active Ingredient(s): | 3; 10; 5; 5; 5 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL & nbsp; avobenzone, homosalate, octisalate, octocrylene, oxybenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51531-4250 |
Labeler Name: | Mary Kay Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120316 |
Package NDC: | 51531-4250-4 |
Package Description: | 1 TUBE in 1 CARTON (51531-4250-4) > 118 mL in 1 TUBE |
NDC Code | 51531-4250-4 |
Proprietary Name | Mary Kay Suncare Sunscreen Broad Spectrum SPF 50 |
Package Description | 1 TUBE in 1 CARTON (51531-4250-4) > 118 mL in 1 TUBE |
Product NDC | 51531-4250 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | avobenzone, homosalate, octisalate, octocrylene, oxybenzone |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20120316 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Mary Kay Inc. |
Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
Strength Number | 3; 10; 5; 5; 5 |
Strength Unit | g/100mL; g/100mL; g/100mL; g/100mL; g/100mL |
Pharmaceutical Classes |