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Hannaford Hand Sanitizer (Health-Tech, Inc.)

Available Formats

Dosage Form Package Information Links
SPRAY 6 CARTON in 1 CASE (48871-002-01) > 12 BLISTER PACK in 1 CARTON > 1 BOTTLE, SPRAY in 1 BLISTER PACK > 7.5 mL in 1 BOTTLE, SPRAY Label Information

Complete Hannaford Hand Sanitizer Information

  • Active Ingredient

    Ethyl alcohol



  • Uses

    • For hand sanitizing to decrease bacteria on the skin.
    • Recommended for repeated use.

  • Warnings

    • For external use only.
    • Do not use in eye area.

    Flammable: Keep away from heat or flame.

  • When using this product

    • Keep out of eyes. In case of eye contact, flush eyes thoroughly with water.
    • Avoid contact with broken skin.

  • Stop use and ask a doctor if

    Irritation or redness develops or if condition persists for more than 72 hours.

  • Keep out of reach of children

    If swallowed, get medical help, or contact a Poison control Center immediately.

  • Directions

    • Pump one to three sprays onto palms of hands
    • Rub thoroughly over all surfaces of both hands
    • Rub hands together briskly until dry
    • Children under 6 should be supervised when using this product
    • Not recommended for infants

  • Other information

    • Store at 200 to 250 C (680 to 770 F)
    • Prior to initial use, prime pump by depressing multiple times
    • May discolor certain fabrics
    • harmful to wood finishes and plastics

  • Inactive Ingredients

    Aloe Vera, D and C Green 5, DI Water, FD and C Yellow 5, Fragrance, Propylene Glycol, Tocopheryl Acetate

  • Hannaford bottle label

    MM9Hannaford bottle label

  • Hannaford blister card

    MM10Hannaford blister card

  • Hannaford shipper label

    MM11Hannaford shipping label

    ethyl alcohol spray
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:48871-002
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    alcohol (UNII: 3K9958V90M) (alcohol - UNII:3K9958V90M) alcohol 4.65 mL  in 7.5 mL
    Inactive Ingredients
    Ingredient Name Strength
    aloe vera leaf (UNII: ZY81Z83H0X)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    water (UNII: 059QF0KO0R)  
    Product Characteristics
    Color green (D and C green 5) , yellow (FD and C yellow 5) Score     
    Shape Size
    Flavor Imprint Code
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:48871-002-01 6 in 1 CASE
    1 12 in 1 CARTON
    1 1 in 1 BLISTER PACK
    1 7.5 mL in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333 03/31/2010
    Labeler - Health-Tech, Inc. (084007889)
    Name Address ID/FEI Business Operations
    Health-Tech, Inc. 084007889 manufacture