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up and up cold and hot medicated (Target Corporation)

Available Formats

Dosage Form Package Information Links
PATCH 1 POUCH in 1 CARTON (11673-818-02) > 5 PATCH in 1 POUCH Label Information
PATCH 1 POUCH in 1 CARTON (11673-818-01) > 5 PATCH in 1 POUCH Label Information

Complete up and up cold and hot medicated Information

  • ACTIVE INGREDIENT

    Active ingredient                                                               Purpose

    Menthol 5%.................................................................... Topical analgesic


  • PURPOSE

    Uses

    Temporarily relieves minor pain associated with:

    • arthritis
    • simple backache
    • bursitis
    • tendonitis
    • muscle strains
    • muscle sprains
    • bruises
    • cramps

  • WARNINGS

    Warnings

    For external use only


  • WHEN USING

    When using this product

    • use only as directed
    • do not bandage tightly or use with a heating pad
    • avoid cotnact with eyes and mucous membranes
    • do not apply to wounds or damaged skin

  • STOP USE

    Stop use and ask a doctor if

    • condition worsens
    • symptoms persist for more than 7 days or clear up and occur again within a few days
    • redness is present
    • skin irritation develops

  • PREGNANCY OR BREAST FEEDING

    If pregnant or breast-feeding, ask a health professional before use


  • KEEP OUT OF REACH OF CHILDREN

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


  • INDICATIONS & USAGE

    Directions

    adult and children under 12 years of age and older:

    • carefully peel off protective backing
    • apply sticky side to affected area
    • wear one patch up to 8 hours
    • repeat as necessary but no more than 3 times daily

    children under 12 years of age:

    • ├»┬╗┬┐consult a doctor

  • STORAGE AND HANDLING

    Other information

    • store at room temperature, not to exceed 86°F (30°C)

  • INACTIVE INGREDIENT

    Inactive ingredients

    1-3-butylene glycol, aloe vera, BHT, d-sorbitol, disodium edetate, gelatin, glycerine, kaolin, liquid paraffin, magnesium aluminium hydrate, methacrylic acid butylacrylate copolymer, methyl parahydroxybenzoate, polysorbate 80, purified water, sodium metaphosphate, sodium polyacrylate, sorbitan monooleate, tartaric acid, titanium dioxide, tocopherol acetate


  • DOSAGE & ADMINISTRATION

    Distributed by:

    Target Corporation

    Minneapolis, MS 55403

    Made in Korea


  • INGREDIENTS AND APPEARANCE
    UP AND UP HOT AND COLD MEDICATED 
    menthol patch
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-818
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 50 mg  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    SORBITOL (UNII: 506T60A25R)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    GELATIN (UNII: 2G86QN327L)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    KAOLIN (UNII: 24H4NWX5CO)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    MAGALDRATE (UNII: 6V88E24N5T)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM METAPHOSPHATE (UNII: 532IUT7IRV)  
    SORBITAN MONOOLEATE (UNII: 06XEA2VD56)  
    TARTARIC ACID (UNII: W4888I119H)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:11673-818-01 1 in 1 BOX 02/07/2017
    1 5 g in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part348 02/23/2015
    Labeler - Target Corp (006961700)