EVOKE ANTIPERSPIRANT AND DEODORANT ROLL-ON - aluminum chlorohydrate liquid 
PSS World Medical

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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EVOKE Antiperspirant & Deodorant Roll On

Active Ingredient

Aluminum chlorohydrate 7.8%

Purpose

Antiperspirant

Uses

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 to underarms only.

Inactive Ingrdients

Ceteareth-20, Cetyl alcohol, fragrance, isopropyl palmitate, magnesium aluminum silicate, methylparaben, mineral oil, propylparaben, sodium benzoate, water.

NDC 68345-850-20

EVOKE

Antiperspirant and

Deodorant Roll On

Lightly scented



Net Contents

1.5fl oz (44.36 mL)



comments or quetions about Evoke products? 800-777-4908

Manufactured for PSS World Medical Inc.

4345 Southpoint Blvd. Jacksonville, FL 32216

Made in Malaysia


Evoke Roll On

EVOKE ANTIPERSPIRANT AND DEODORANT ROLL-ON 
aluminum chlorohydrate liquid
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:68345-850
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM CHLOROHYDRATE (ALUMINUM CHLOROHYDRATE) ALUMINUM CHLOROHYDRATE7.8 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
POLYOXYL 20 CETOSTEARYL ETHER 
CETYL ALCOHOL 
ISOPROPYL PALMITATE 
MAGNESIUM ALUMINUM SILICATE 
METHYLPARABEN 
MINERAL OIL 
PROPYLPARABEN 
SODIUM BENZOATE 
WATER 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68345-850-2044.36 mL in 1 BOTTLE, WITH APPLICATOR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35006/15/2011
Labeler - PSS World Medical (101822682)

Revised: 6/2011
 
PSS World Medical