XTRACARE ANTIFUNGAL FOOT- tolnaftate spray 
Taizhou Ludao Cosmetics Co., Ltd.

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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Antifungal Spray

Active Ingredient  ............................................ Purpose

Tolnaftate 1% .................................................. Antifungal

Use

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately. Do not use on children under 2 years of age unless directed by a doctor.

XtraCare® Antifungal Foot Spray

For Athlete's Foot

Tolnaftate 1%

*Compare to the Active Ingredient in Tinactin®

CAUTION  Contents under pressure - Read precautions on back panel.

Net Wt 3.5 Oz (100g)

Warnings

For external use only.

Flammable. Do not use while smoking or near heat or flame. Do not puncture or incinerate. Contents under pressure. Do not store at temperatures above 120oF (49oC).

When using this product

Stop use and ask a doctor if

Directions

Inactive Ingredients

butane, propane, alcohol, butylated hydroxytoluene, talc.

Other information store between 68o to 77oF (20o to 25oC)

Questions/Comments? 1-855-345-5575

*This product is not manufactured or distributed by Schering-Plough HealthCare Products, Inc., owner of the registered trademark Tinactin®

DISTRIBUTED BY

REJOICE INTERNATIONAL, INC

NORTHVILLE, MI 48168 USA

MADE IN CHINA

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XTRACARE ANTIFUNGAL FOOT 
tolnaftate spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50942-001
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
BUTANE (UNII: 6LV4FOR43R)  
PROPANE (UNII: T75W9911L6)  
ALCOHOL (UNII: 3K9958V90M)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
TALC (UNII: 7SEV7J4R1U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50942-001-01100 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product02/11/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C02/11/2014
Labeler - Taizhou Ludao Cosmetics Co., Ltd. (679885595)
Establishment
NameAddressID/FEIBusiness Operations
Taizhou Ludao Cosmetics Co., Ltd.679885595manufacture(50942-001)

Revised: 12/2018
Document Id: 7d7b6448-0773-d3c3-e053-2991aa0a45bd
Set id: 5fd847da-78c4-41e9-af18-a2e9a454aa01
Version: 2
Effective Time: 20181220
 
Taizhou Ludao Cosmetics Co., Ltd.