Product NDC: | 0316-2035 |
Proprietary Name: | Blue Lizard Baby |
Non Proprietary Name: | Titanium Dioxide and Zinc Oxide |
Active Ingredient(s): | 54; 108 mg/mL; mg/mL & nbsp; Titanium Dioxide and Zinc Oxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0316-2035 |
Labeler Name: | Crown Laboratories |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20031208 |
Package NDC: | 0316-2035-30 |
Package Description: | 89 mL in 1 TUBE (0316-2035-30) |
NDC Code | 0316-2035-30 |
Proprietary Name | Blue Lizard Baby |
Package Description | 89 mL in 1 TUBE (0316-2035-30) |
Product NDC | 0316-2035 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Titanium Dioxide and Zinc Oxide |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20031208 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Crown Laboratories |
Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | 54; 108 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |