Medication Guide App

Old Spice Red Zone Sweat Defense After Hours

Dosage form: stick
Ingredients: Aluminum Zirconium Trichlorohydrex Gly 0.19g in 1g
Labeler: Procter & Gamble Manufacturing Company
NDC Code: 37000-180

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.

Old Spice®
SWEAT
DEFENSE
AFTER HOURS

Drug Facts

Active ingredient

Aluminum zirconium trichlorohydrex Gly 19% (anhydrous)

Purpose

Antiperspirant

Use

reduces underarm wetness

Warnings

For external use only.

Do not use on broken skin

Ask a doctor before use if you have kidney disease

Stop use if rash or irritation occurs

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions
  • apply to underarms only

Inactive ingredients

cyclopentasiloxane, dimethicone, tribehenin, fragrance, C18-36 acid triglyceride

QUESTIONS?

1-800-677-7582

www.oldspice.com

Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202.

PRINCIPAL DISPLAY PANEL - 73 g container

Old Spice®

SWEAT
DEFENSE

EXTRA STRONG
ANTI-PERSPIRANT
& DEODORANT

AFTER HOURS

GIVING SWEAT A BEAT DOWN

ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
ANTI-PERSPIRANT/DEODORANT

NET WT.
2.6 OZ (73 g)

99286644

OLD SPICE RED ZONE SWEAT DEFENSE   AFTER HOURS
aluminum zirconium trichlorohydrex gly stick
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-180
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Aluminum Zirconium Trichlorohydrex Gly (Aluminum Cation) Aluminum Zirconium Trichlorohydrex Gly0.19 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
cyclomethicone 5 
dimethicone 
tribehenin 
C18-36 acid triglyceride 
Product Characteristics
ColorWHITEScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:37000-180-7373 g in 1 CANISTER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart35012/01/2009
Labeler - Procter & Gamble Manufacturing Company (004238200)
Establishment
NameAddressID/FEIOperations
Procter & Gamble Manufacturing Company017745779MANUFACTURE

Revised: 12/2010
 
Procter & Gamble Manufacturing Company

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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