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UV Shield SPF 42
UV Shield SPF 42 - 75847-9001-1 - (OCTINOXATE)
Drug Information of UV Shield SPF 42
| Product NDC: | 75847-9001 |
| Proprietary Name: | UV Shield SPF 42 |
| Non Proprietary Name: | OCTINOXATE |
| Active Ingredient(s): | .075 mL/mL & nbsp; OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of UV Shield SPF 42
| Product NDC: | 75847-9001 |
| Labeler Name: | IASO Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110109 |
Package Information of UV Shield SPF 42
| Package NDC: | 75847-9001-1 |
| Package Description: | 70 mL in 1 BOTTLE (75847-9001-1) |
NDC Information of UV Shield SPF 42
| NDC Code | 75847-9001-1 |
| Proprietary Name | UV Shield SPF 42 |
| Package Description | 70 mL in 1 BOTTLE (75847-9001-1) |
| Product NDC | 75847-9001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20110109 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | IASO Inc |
| Substance Name | OCTINOXATE |
| Strength Number | .075 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |
