HAND SANITIZER- alcohol gel 
Target Corporation

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.

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Active Ingredient

Alcohol 62%

Purpose

Antiseptic

Use

■ For handwashing to decrease bacteria on the skin ■ Recommended for repeated use

Warnings

For external use only

■ Flammable, keep away from fire & flame

■ Does not contain grain alcohol;do not drink. If taken internally will produce serious gastric disturbances

When using this product

■ Avoid the eyes and mucous membranes

■ In the case of eyes or mucous membranes contact, rinse area thoroughly with water

Stop use and ask a doctor if

■ Condition worsens

■ Redness or irritation develops

■ If condition persists for more than 3 days

Keep out of reach of children

■ If swallowed contact a doctor or Poison Control Center immediately.

Directions

■ Rub dime sized amount between hands until dry

■ Supervise children in the use of this product

■ In the case of eye contact, rinse eyes thoroughly with water

Other information

■ Store below 105°F ■ May discolor some fabrics

Inactive Ingredients

Water, Glycerin, Fragrance, Carbomer, Aminomethyl Propanol, Denatonium Benzoate, Red 40, Yellow 5

Questions?

■ 1-800-278-9218

Package Label Red

package label red

HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-258
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
GLYCERIN (UNII: PDC6A3C0OX)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
WATER (UNII: 059QF0KO0R)  
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-258-3030 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A07/01/2020
Labeler - Target Corporation (006961700)

Revised: 7/2020
Document Id: a9c8c672-bb0f-12df-e053-2a95a90ad204
Set id: a9c8ccc2-1654-1594-e053-2995a90aca1c
Version: 1
Effective Time: 20200706
 
Target Corporation