SWEET SUGAR FANTASY HAND SANITIZER ANTIBACTERIAL- alcohol gel 
Core Home

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.

----------

CoreXiamenWallyBluelHndSntzrAlch70

Active ingredient

Alcohol 70%

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 and flame

Does not contain grain alcohol, do not drink. If taken internally will produce gastric distrubances.

When using this product

■ Avoid the eyes and mucoous membranes

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

Stop use and ask a doctor if

■ Condition worsens

■ Redness or irritation develops

■ 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 105ºF

■ May discolor some fabrics.

Inactive ingredients

Water, Glycerin, PEG-40 Hydrogenated Castor Oil, Carbomer, Fragrance, Aminomethyl Propanol, Blue 1, Yellow 5

Questions?

■ 1-800-278-9218

Package Label

package label

SWEET SUGAR FANTASY HAND SANITIZER  ANTIBACTERIAL
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80424-006
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
WATER (UNII: 059QF0KO0R)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:80424-006-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product04/21/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A04/21/2021
Labeler - Core Home (831309427)

Revised: 4/2021
Document Id: c0834c25-7475-d7b6-e053-2995a90ad9cb
Set id: c0831247-f0e5-aea1-e053-2995a90ae405
Version: 1
Effective Time: 20210423
 
Core Home