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UltraMax Roll On
UltraMax Roll On - 10237-900-19 - (Aluminum Zirconium Tetrachlorohydrex Gly)
Drug Information of UltraMax Roll On
| Product NDC: | 10237-900 |
| Proprietary Name: | UltraMax Roll On |
| Non Proprietary Name: | Aluminum Zirconium Tetrachlorohydrex Gly |
| Active Ingredient(s): | 21 g/100mL & nbsp; Aluminum Zirconium Tetrachlorohydrex Gly |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of UltraMax Roll On
| Product NDC: | 10237-900 |
| Labeler Name: | Church & Dwight Co., Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20000728 |
Package Information of UltraMax Roll On
| Package NDC: | 10237-900-19 |
| Package Description: | 56 mL in 1 BOTTLE, WITH APPLICATOR (10237-900-19) |
NDC Information of UltraMax Roll On
| NDC Code | 10237-900-19 |
| Proprietary Name | UltraMax Roll On |
| Package Description | 56 mL in 1 BOTTLE, WITH APPLICATOR (10237-900-19) |
| Product NDC | 10237-900 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aluminum Zirconium Tetrachlorohydrex Gly |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20000728 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Church & Dwight Co., Inc. |
| Substance Name | ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY |
| Strength Number | 21 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |
