ATHLETES FOOT DR FOOT- tolnaftate aerosol 
Blue Cross Laboratories

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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Athletes Foot Spray

Active Ingredients                   Purpose

w/w Tolnaftate 1%                  antifungal

Uses

for relief of itching and burning

cures and prevents most athlete's foot

Keep out of reach of children.

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

Stop use and ask a doctor if

condition worsens

symptoms persist for more than 10 days or irritation occurs

Do not use

- in the eyes

- on nail or scalp infections

Directions

Adults and children 2 years of age and older: cleanse skin with soap and water and dry thoroughly.

Shake can well; hold 6 inches away and spray on feet and between toes morning and night for full treatment period (4 weeks) even if symptoms disappear.

Should the spray dispenser become clogged, clean the spraying hole with a needle.

Wear well-fitting, ventilated shoes and cotton socks.

Children under 2 years of age: consult a doctor.

Change shoes and socks at least once a day.


Inactive ingredients

Alcohol SD 40-B, isobutane (propellant), talc


image of Secondary label

Dr. Foot tm  Athletes' Foot Spray

Net Wt. 4 oz. (113 g)


image of Primary Label

ATHLETES FOOT  DR FOOT
tolnaftate aerosol
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:22431-576
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
ISOBUTANE (UNII: BXR49TP611)  
TALC (UNII: 7SEV7J4R1U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22431-576-021 in 1 BOX10/19/201008/01/2017
1NDC:22431-576-01113 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C10/19/201008/01/2017
Labeler - Blue Cross Laboratories (008298879)
Registrant - Blue Cross Laboratories (008298879)
Establishment
NameAddressID/FEIBusiness Operations
Ninghai Everstar Co. Ltd.527072149manufacture(22431-576)

Revised: 8/2017
 
Blue Cross Laboratories