Drug Facts

Drug Facts

Drug Labeling and Warnings

Drug Details

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ULTRAMAX  ANTIPERSPIRANT DEODORANT COOL BLAST- aluminum zirconium tetrachlorohydrex gly gel 
Church & Dwight Co., Inc.

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.

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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

Apply a thin layer to underarms only.

Inactive ingredients

Water, Cyclopentasiloxane, SD alcohol 40, Propylene Glycol, Dimethicone, PEG/PPG-18/18 Dimethicone, Sodium Bicarbonate (Baking Soda), Fragrance

Principal Display

Arm and Hammer
The Standard of Purity


ULTRA MAX
Antiperspirant
Deodorant

CLEAR GEL

Cool Blast

NET WT.4.0OZ. (113g)

Carton ImageCarton Image

ULTRAMAX   ANTIPERSPIRANT DEODORANT COOL BLAST
aluminum zirconium tetrachlorohydrex gly gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 10237-805
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY19 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
ALCOHOL (UNII: 3K9958V90M)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
POLYETHYLENE GLYCOL 900 (UNII: UEP843BRCQ)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 10237-805-40113 g in 1 CANISTER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35012/01/2003
Labeler - Church & Dwight Co., Inc. (001211952)
Establishment
NameAddressID/FEIBusiness Operations
Church & Dwight Co., Inc.043690812manufacture

Revised: 8/2011
 
Church & Dwight Co., Inc.


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