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Lacura Extreme Blast
Lacura Extreme Blast - 10889-110-17 - (ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY)
Drug Information of Lacura Extreme Blast
| Product NDC: | 10889-110 |
| Proprietary Name: | Lacura Extreme Blast |
| Non Proprietary Name: | ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY |
| Active Ingredient(s): | 250 mg/g & nbsp; ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY |
| Administration Route(s): | CUTANEOUS |
| Dosage Form(s): | STICK |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lacura Extreme Blast
| Product NDC: | 10889-110 |
| Labeler Name: | VVF Kansas Services LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20101213 |
Package Information of Lacura Extreme Blast
| Package NDC: | 10889-110-17 |
| Package Description: | 76 g in 1 PACKAGE (10889-110-17) |
NDC Information of Lacura Extreme Blast
| NDC Code | 10889-110-17 |
| Proprietary Name | Lacura Extreme Blast |
| Package Description | 76 g in 1 PACKAGE (10889-110-17) |
| Product NDC | 10889-110 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY |
| Dosage Form Name | STICK |
| Route Name | CUTANEOUS |
| Start Marketing Date | 20101213 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | VVF Kansas Services LLC |
| Substance Name | ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY |
| Strength Number | 250 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
