JOCK ITCH- tolnaftate spray 
Walgreen Company

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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Walgreen Co. Jock Itch Powder Spray Drug Facts

Active ingredient

Tolnaftate 1%

Purpose

Antifungal

Uses

cures most jock itch
for effective relief of itching, chafing and burning

Warnings

For external use only

Flammable: Do not use while smoking or near heat or flame

Do not use

on children under 2 years of age unless directed by a doctor

When using this product

avoid contact with the eyes
use only as directed. Intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal.
contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120°F (49°C).

Stop use and ask a doctor if

irritation occurs
there is no improvement within 2 weeks

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Directions

wash affected area and dry thoroughly
shake can well and spray a thin layer over affected area twice daily (morning and night)
supervise children in the use of this product
use daily for 2 weeks; if condition persists longer, ask a doctor
this product is not effective on the scalp or nails
in case of clogging, clean nozzle with a pin

Other information

store at 20-25°C (68-77°F)

Inactive ingredients

alcohol denat., aluminum starch octenylsuccinate, isobutane, isopropyl myristate, propylene carbonate, sorbitan monooleate, stearalkonium hectorite, talc

Questions or comments?

1-800-719-9260

Package/Label Principal Display Panel

Compare to Tinactin® active ingredient

Jock Itch Powder Spray

TOLNAFTATE 1% / ANTIFUNGAL

MAXIMUM STRENGTH

Cures most jock itch

Soothes & relieves itching, burning & chafing

NET WT 4.6 OZ (130 g)

jock itch image
JOCK ITCH 
tolnaftate spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0695
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
ISOBUTANE (UNII: BXR49TP611)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
SORBITAN MONOOLEATE (UNII: 06XEA2VD56)  
STEARALKONIUM HECTORITE (UNII: OLX698AH5P)  
TALC (UNII: 7SEV7J4R1U)  
Product Characteristics
ColorWHITE (off-white) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-0695-90130 g in 1 CAN; Type 0: Not a Combination Product06/08/2005
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C06/08/2005
Labeler - Walgreen Company (008965063)

Revised: 10/2020
Document Id: ae539fc7-1fa6-48d3-8de8-88c30699d6b3
Set id: c86ab353-75fb-496c-a812-04a0679edaf7
Version: 6
Effective Time: 20201013
 
Walgreen Company