TING- tolnaftate cream 
Insight Pharmaceuticals LLC

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.

----------

Ting

Drug Facts

TING Antifungal Cream

Active ingredient

Tolnaftate 1%

Purpose

Antifungal

Uses

Warnings

For external use only

Do not use

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

When using this product avoid contact with the eyes

Stop use and ask a doctor if

  • Irritation occurs or if there is no improvement within 4 weeks (for athlete's foot and ringworm)
  • Irritation occurs or if there is no improvement within 2 weeks (for jock itch)

Keep out of reach of children

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

Directions

For athlete's foot use daily for 4 weeks. If condition persists longer, consult a doctor.

For ringworm use daily for 4 weeks. If condition persists longer, consult a doctor.

For jock itch use daily for 2 weeks. If condition persists longer, consult a doctor.

This product is not effective on the scalp or nails.

Inactive ingredients

Butylated Hydroxytoluene, PEG-400, PEG-3350, Titanium Dioxide, White Petrolatum

Principal Display Panel

TING
TOLNAFTATE
ANTIFUNGAL
CREAM

NET WT. 0.5 oz (14 g)

TING Antifungal Cream Carton

TING 
tolnaftate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63736-051
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE10 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
PETROLATUM (UNII: 4T6H12BN9U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63736-051-011 in 1 BOX06/08/2009
114 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C06/08/2009
Labeler - Insight Pharmaceuticals LLC (055665422)

Revised: 3/2018
Document Id: 588715b9-e752-4e8f-a0a5-4f157ad160a3
Set id: bc89b8ec-4f9d-42d8-a38c-9b6284a54a34
Version: 2
Effective Time: 20180301
 
Insight Pharmaceuticals LLC