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UltraMax Roll On - 10237-900-19 - (Aluminum Zirconium Tetrachlorohydrex Gly)

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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

Complete Information of UltraMax Roll On


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