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Hannaford Hand Sanitizer

Medically reviewed on March 23, 2018

Dosage form: spray
Ingredients: alcohol 4.65mL in 7.5mL
Labeler: Health-Tech, Inc.
NDC Code: 48871-002

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 Facts

Active Ingredient

Ethyl alcohol

Purpose

Antiseptic

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

MM9

Hannaford blister card

MM10

Hannaford shipper label

MM11

HANNAFORD HAND SANITIZER  
ethyl alcohol spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48871-002
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
alcohol (alcohol) alcohol4.65 mL  in 7.5 mL
Inactive Ingredients
Ingredient NameStrength
aloe vera leaf 
ALPHA-TOCOPHEROL ACETATE 
Propylene Glycol 
water 
Product Characteristics
Colorgreen (D and C green 5) , yellow (FD and C yellow 5) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:48871-002-016 CARTON (CARTON) in 1 CASE
112 BLISTER PACK (BLISTER PACK) in 1 CARTON
11 BOTTLE, SPRAY (BOTTLE) in 1 BLISTER PACK
17.5 mL in 1 BOTTLE, SPRAY
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33303/31/2010
Labeler - Health-Tech, Inc. (084007889)
Establishment
NameAddressID/FEIOperations
Health-Tech, Inc.084007889manufacture

 
Health-Tech, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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