Product NDC: | 43948-8001 |
Proprietary Name: | Medi UV Block Suncream SPF50 PA |
Non Proprietary Name: | OCTINOXATE OCTOCRYLENE |
Active Ingredient(s): | 3; .6 mL/60mL; mL/60mL & nbsp; OCTINOXATE OCTOCRYLENE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43948-8001 |
Labeler Name: | The Doctor's Cosmetic Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20091101 |
Package NDC: | 43948-8001-1 |
Package Description: | 60 mL in 1 TUBE (43948-8001-1) |
NDC Code | 43948-8001-1 |
Proprietary Name | Medi UV Block Suncream SPF50 PA |
Package Description | 60 mL in 1 TUBE (43948-8001-1) |
Product NDC | 43948-8001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE OCTOCRYLENE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20091101 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | The Doctor's Cosmetic Inc |
Substance Name | OCTINOXATE; OCTOCRYLENE |
Strength Number | 3; .6 |
Strength Unit | mL/60mL; mL/60mL |
Pharmaceutical Classes |