Label: HAND SANITIZER ORANGE TANGERINE- alcohol liquid 

  • Label RSS
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

NOTE: Most over the counter (OTC) are not reviewed and approved by the 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 11/12

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    ​Drug Facts

    ​Active Ingredient

    Ethyl Alcohol 63%

    Purpose

    Anticeptic

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  • PURPOSE

    ​Uses

    ​To decrease bacteria on the skin.

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  • WARNINGS

    ​Warning

    For external use only.

    Flammable.

    Keep away from heat and flame.

    When using this product

    • Avoid contact with eyes. If contact occurs, flush eyes with water.
    • Avoid contact with broken skin.

    Stop use and consult a doctor if irritation and reness develop and persis for more than 72 hours.

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  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

    In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

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  • INDICATIONS & USAGE

    Directions

    ■ Wet hands with product and allow to dry without wiping.
    ■ Not recommended for infants.

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  • OTHER SAFETY INFORMATION

    Other Information

    ■ Store at 68 o to 77 oF (20 o to 25 oc).
    ■ Do not store above 105 oF.
    ■ May discolor some fabrics.
    ■ Harmful to wood finishes and plastics.

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  • INACTIVE INGREDIENT

    Inactive Ingredient

    Alcohol Denat., Water, Propylene Glycol, Fragrance, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Lactose, Cellulose, Hydroxypropyl Methylcellulose, Jojoba Esters, Tocopheryl Acetate, Blue 1(CI 42090), Red 33(CI 17200), Red 4(CI 14700).

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  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER  ORANGE TANGERINE
    alcohol liquid
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:49035-217(NDC:51706-500)
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALCOHOL (ALCOHOL) ALCOHOL 62 mL  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    Water 1 mL  in 100 mL
    PROPYLENE GLYCOL 1 mL  in 100 mL
    TROLAMINE 1 mL  in 100 mL
    HYPROMELLOSES 1 mL  in 100 mL
    CELLULOSE, MICROCRYSTALLINE 1 mL  in 100 mL
    HYDROXYPROPYL METHYLCELLULOSE E5 [II] 1 mL  in 100 mL
    FD&C YELLOW NO. 5 1 mL  in 100 mL
    FD&C BLUE NO. 1 1 mL  in 100 mL
    FD&C RED NO. 4 1 mL  in 100 mL
    Product Characteristics
    Color blue, red Score     
    Shape Size
    Flavor Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:49035-217-01 29 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333E 11/01/2012
    Labeler - Wal-Mart Stores Inc. (051957769)
    Registrant - Wal-Mart Stores Inc. (051957769)
    Establishment
    Name Address ID/FEI Business Operations
    Landy International 545291775 manufacture(49035-217)
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