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Blue Lizard Face
Blue Lizard Face - 0316-2055-20 - (Sunscreen)
Drug Information of Blue Lizard Face
| Product NDC: | 0316-2055 |
| Proprietary Name: | Blue Lizard Face |
| Non Proprietary Name: | Sunscreen |
| Active Ingredient(s): | 55; 80 mg/g; mg/g & nbsp; Sunscreen |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Blue Lizard Face
| Product NDC: | 0316-2055 |
| Labeler Name: | Crown Laboratories |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100406 |
Package Information of Blue Lizard Face
| Package NDC: | 0316-2055-20 |
| Package Description: | 35.4 g in 1 BOTTLE, PLASTIC (0316-2055-20) |
NDC Information of Blue Lizard Face
| NDC Code | 0316-2055-20 |
| Proprietary Name | Blue Lizard Face |
| Package Description | 35.4 g in 1 BOTTLE, PLASTIC (0316-2055-20) |
| Product NDC | 0316-2055 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sunscreen |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20100406 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Crown Laboratories |
| Substance Name | OCTINOXATE; ZINC OXIDE |
| Strength Number | 55; 80 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
