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UltraMax Roll On Antiperspirant Deodorant Powder Fresh

Dosage form: liquid
Ingredients: ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY 21g in 100mL
Labeler: Church & Dwight Co., Inc.
NDC Code: 10237-900

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Facts

Active ingredient

Aluminum Zirconium Tetrachlorohydrex Gly (19%)

Purpose

Antiperspirant

Use

reduces underarm perspiration

Warnings For external use only

Do not use on broken skin

Stop use if rash or irritation occurs

Ask a doctor before use if you have kidney disease

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Shake well. Apply a thin layer to underarms only.

Inactive ingredients

Cyclopentasiloxane, Sodium Bicarbonate (Baking Soda), Disteardimonium Hectorite, Fragrance, Propylene Carbonate, Silica, corn Starch Modified, Polysaccharides, Maltodextrin.

Principal Display

Arm and Hammer
The Standard of Purity


ULTRA MAX
Antiperspirant
Deodorant


1.9 Fl. OZ. (56mL)

POWDER FRESH

Carton Image UMLBF-LB19130-04-06

ULTRAMAX ROLL ON  ANTIPERSPIRANT DEODORANT POWDER FRESH
aluminum zirconium tetrachlorohydrex gly liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10237-900
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (ALUMINUM CATION) ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY21 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CYCLOMETHICONE 5 
SODIUM BICARBONATE 
HECTORITE  
PROPYLENE CARBONATE 
SILICON DIOXIDE 
STARCH, CORN 
XANTHAN GUM 
MALTODEXTRIN 
Packaging
#Item CodePackage Description
1NDC:10237-900-1956 mL in 1 BOTTLE, WITH APPLICATOR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35007/28/2000
Labeler - Church & Dwight Co., Inc. (001211952)
Establishment
NameAddressID/FEIOperations
Church & Dwight Canada Corp253933600manufacture(10237-900)

Revised: 03/2013
 
Church & Dwight Co., Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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