| 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 |