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Sweet Sugar Fantasy Hand Sanitizer by

Drug Labeling and Warnings

Sweet Sugar Fantasy Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Core Home. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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.

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Active ingredient

Alcohol 63%

Purpose

Antiseptic

Uses

■ 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

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance, PEG-40 Hydrogenated Castor Oil, Water

Questions?

■ 1-800-278-9218

Package Label

SWEET SUGAR FANTASY HAND SANITIZER  ANTIBACTERIAL
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80424-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	63 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
WATER (UNII: 059QF0KO0R)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80424-010-01	3 in 1 BLISTER PACK	05/05/2021	05/17/2023
1	NDC: 80424-010-30	30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/05/2021	05/17/2023

Labeler - Core Home (831309427)

Revised: 7/2022

Document Id: e38da1e7-7810-15eb-e053-2a95a90a6296

34390-5

Set id: c23c754a-944e-0a05-e053-2995a90afc55

Version: 2

Effective Time: 20220711