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LBEL
LBEL - 13537-501-02 - (Titanium Dioxide, Zinc Oxide, and Octinoxate)
Drug Information of LBEL
| Product NDC: | 13537-501 |
| Proprietary Name: | LBEL |
| Non Proprietary Name: | Titanium Dioxide, Zinc Oxide, and Octinoxate |
| Active Ingredient(s): | .03; .062393; .049 g/g; g/g; g/g & nbsp; Titanium Dioxide, Zinc Oxide, and Octinoxate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LBEL
| Product NDC: | 13537-501 |
| Labeler Name: | Ventura Corporation LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130527 |
Package Information of LBEL
| Package NDC: | 13537-501-02 |
| Package Description: | 1 CARTRIDGE in 1 BOX (13537-501-02) > 10 g in 1 CARTRIDGE (13537-501-01) |
NDC Information of LBEL
| NDC Code | 13537-501-02 |
| Proprietary Name | LBEL |
| Package Description | 1 CARTRIDGE in 1 BOX (13537-501-02) > 10 g in 1 CARTRIDGE (13537-501-01) |
| Product NDC | 13537-501 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Titanium Dioxide, Zinc Oxide, and Octinoxate |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20130527 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Ventura Corporation LTD. |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | .03; .062393; .049 |
| Strength Unit | g/g; g/g; g/g |
| Pharmaceutical Classes |
