Sweet Sugar Fantasy Hand Sanitizer

Manufacturer
Core Home
Effective date
2022-07-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:56:58

Label at a glance#

ProductSweet Sugar Fantasy Hand Sanitizer ANTIBACTERIAL
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

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

Dosage and administration

■ 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.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 63%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

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

OTC - WHEN USING SECTION

■ 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

OTC - STOP USE SECTION

■ Condition worsens

■ Redness or irritation develops

■ Condition persists for more than 3 days

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

■ 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

SPL UNCLASSIFIED SECTION

■ Store below 105ºF

■ May discolor some fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Questions?

OTC - QUESTIONS SECTION

■ 1-800-278-9218

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

inner package labelinner package label

Products#

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DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80424-01080424-010-30, 80424-010-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
e38da1e7-7810-15eb-e053-2a95a90a6296c23c754a-944e-0a05-e053-2995a90afc552022-07-11WarningsExact identifier
spl id: e38da1e7-7810-15eb-e053-2a95a90a6296
spl set id: c23c754a-944e-0a05-e053-2995a90afc55

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.