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Blue Lizard Regular
Blue Lizard Regular - 0316-2010-30 - (Sunscreen)
Drug Information of Blue Lizard Regular
| Product NDC: | 0316-2010 |
| Proprietary Name: | Blue Lizard Regular |
| Non Proprietary Name: | Sunscreen |
| Active Ingredient(s): | 76.5; 20.4; 30.6; 61.2 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Sunscreen |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Blue Lizard Regular
| Product NDC: | 0316-2010 |
| Labeler Name: | Crown Laboratories |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20010415 |
Package Information of Blue Lizard Regular
| Package NDC: | 0316-2010-30 |
| Package Description: | 89 mL in 1 TUBE (0316-2010-30) |
NDC Information of Blue Lizard Regular
| NDC Code | 0316-2010-30 |
| Proprietary Name | Blue Lizard Regular |
| Package Description | 89 mL in 1 TUBE (0316-2010-30) |
| Product NDC | 0316-2010 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sunscreen |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20010415 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Crown Laboratories |
| Substance Name | OCTINOXATE; OCTOCRYLENE; OXYBENZONE; ZINC OXIDE |
| Strength Number | 76.5; 20.4; 30.6; 61.2 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
