PROCLEARZ MAXIMUM STRENGTH FUNGAL SHIELD BRUSH-ON ANTIFUNGAL- tolnaftate solution 
Profoot, Inc.

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ProClearz Maximum Strength Fungal Sheild Anti-Fungal Brush-On Solution

Active Ingredient

Tolnaftate 1%

Purpose

Anti-fungal

Uses

Warnings

For external use only

Extremely flammable

When using this product

Stop use and ask a doctor if

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

Directions

■ shake well before using ■ wash affected area and dry thoroughly ■ apply a thin layer of the product over affected area (around the nails and underneath nail tips) twice daily or as directed by a doctor ■ supervise children in the use of this product ■ for athlete’s foot, pay special attention to spaces between the toes; wear well fitting, ventilated shoes and change shoes and socks at least once daily ■ for athlete’s foot and ringworm, use daily for 4 weeks. If condition persists longer, consult a doctor ■ this product is not effective on the scalp or nails




Other Information

Inactive ingredients

Acetone, Aloe Vera (Aloe Barbadensis) Gel, Propylene Glycol, Tocopherol Acetate (Vitamin E), Water

updated outer boxDrug Facts PanelUpated Inner Label

PROCLEARZ  MAXIMUM STRENGTH FUNGAL SHIELD BRUSH-ON ANTIFUNGAL
tolnaftate solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:29784-181
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ACETONE (UNII: 1364PS73AF)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:29784-181-021 in 1 BOX10/22/2012
1NDC:29784-181-0130 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00510/22/2012
Labeler - Profoot, Inc. (107570900)

Revised: 11/2023
Document Id: 0ac47078-d549-277f-e063-6294a90ae934
Set id: 4d451e87-c25b-49cf-92b8-747b053930c2
Version: 34
Effective Time: 20231122
 
Profoot, Inc.