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EGF UV SHIELD
EGF UV SHIELD - 58831-1001-2 - (OCTINOXATE)
Drug Information of EGF UV SHIELD
| Product NDC: | 58831-1001 |
| Proprietary Name: | EGF UV SHIELD |
| Non Proprietary Name: | OCTINOXATE |
| Active Ingredient(s): | 2; 7.5; 5; 4.15; 4.9 g/60g; g/60g; g/60g; g/60g; g/60g & nbsp; OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of EGF UV SHIELD
| Product NDC: | 58831-1001 |
| Labeler Name: | Dermaesthetics Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130626 |
Package Information of EGF UV SHIELD
| Package NDC: | 58831-1001-2 |
| Package Description: | 1 TUBE in 1 BOX (58831-1001-2) > 60 g in 1 TUBE (58831-1001-1) |
NDC Information of EGF UV SHIELD
| NDC Code | 58831-1001-2 |
| Proprietary Name | EGF UV SHIELD |
| Package Description | 1 TUBE in 1 BOX (58831-1001-2) > 60 g in 1 TUBE (58831-1001-1) |
| Product NDC | 58831-1001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130626 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Dermaesthetics Inc. |
| Substance Name | AMILOXATE; OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 2; 7.5; 5; 4.15; 4.9 |
| Strength Unit | g/60g; g/60g; g/60g; g/60g; g/60g |
| Pharmaceutical Classes |
