Label: TING- miconazole nitrate aerosol, powder

  • NDC Code(s): 63736-532-05
  • Packager: Insight Pharmaceuticals LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

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.

Drug Label Information

Updated April 8, 2020

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Miconazole Nitrate 2%

  • Purpose

    Antifungal

  • Uses

     ▪ effective in the treatment of most athlete's foot (tinea pedis), jock itch (tinea cruris) and ringworm (tinea corporis)

    ▪ effectively relieves itching, scaling, burning and discomfort that can accompany athlete's foot and jock itch

  • Warnings

    For external use onlyFlammability Warning:  Contents under pressure. Do not puncture or incinerate. Flammable mixture; do not use near fire or flame, or expose to heat or temperatures above 49°C (120°F). Use only as directed. Intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal.

    When using this product

    avoid contact with the eyes

    Do not use

    ▪ in or near the mouth or the eyes

    ▪ for nail or scalp infections

    Stop use and ask a doctor if

    irritation occurs or if there is no improvement within 4 weeks (for athlete's foot and ringworm) or 2 weeks (for jock itch)Do not use on children under 2 years of unless directed by a doctor.

    Keep out of reach of children.

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

  • Directions

    ▪ clean the affected area and dry thoroughly▪ shake can well, hold  4" to 6" from skin. Spray a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor▪ supervise children in the use of this product. ▪ for athlete's foot, pay special attention to the 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; for jock itch, use daily for 2 weeks. If condition persists longer, consult a doctor.

  • Other information

    Store at room temperature 15°-25°C (59°-77°F).

  • Inactive ingredients

    Aloe vera gel, aluminum starch octenylsuccinate, isopropyl myristate, propylene carbonate, SD alcohol 40-B (10% w/w), sorbitan monooleate, stearalkonium hectorite. Propellant: Isobutane, normal butane, propane

  • Questions?

    1-800-344-7239©2016  Distributed by INSIGHT Pharmaceuticals Corp., a Prestige Brands Company

    Tarrytown, NY 10591Made in India

    TAMPER RESISTANT AEROSOL CAN FOR YOUR PROTECTION

  • Principal display panel:

    Ting ®
    Athlete’s Foot Spray

    2% Miconazole Nitrate
    Antifungal Spray Powder

    Net WT 4.5 oz (128 g)

    Ting ®
Athlete’s Foot Spray

2% Miconazole Nitrate
Antifungal Spray Powder

Net WT 4.5 oz (128 g)

  • INGREDIENTS AND APPEARANCE
    TING 
    miconazole nitrate aerosol, powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63736-532
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE2.56 g  in 128 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
    ALCOHOL (UNII: 3K9958V90M)  
    SORBITAN MONOOLEATE (UNII: 06XEA2VD56)  
    STEARALKONIUM HECTORITE (UNII: OLX698AH5P)  
    ISOBUTANE (UNII: BXR49TP611)  
    BUTANE (UNII: 6LV4FOR43R)  
    PROPANE (UNII: T75W9911L6)  
    Product Characteristics
    ColorWHITEScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63736-532-05128 g in 1 CAN; Type 0: Not a Combination Product07/16/2009
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH FINALpart333C07/16/2009
    Labeler - Insight Pharmaceuticals LLC (055665422)