FDA.reportPublic FDA data

Sweet Sugar Fantasy Hand Sanitizer

Manufacturer
Xiamen Wally Bath Manufacture Co., Ltd
Effective date
2021-04-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:45:54

Label at a glance#

ProductSweet Sugar Fantasy Hand Sanitizer ANTIBACTERIAL
Active ingredientALCOHOL
Label structure12 sections

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 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

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

Water, Glycerin, PEG-40 Hydrogenated Castor Oil, Carbomer, Fragrance, Aminomethyl Propanol, Red 4, Red 33

Questions?

OTC - QUESTIONS SECTION

■ 1-800-278-9218

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78868-008-012025-02-28C16284748780-1f386c649-f3f5-0266-e053-dadaa90a7c1aXiamenCoreWallyPnkHndSntzrAlch70
78868-008-012023-01-30C16284748780-1f386c649-f3f5-0266-e053-dadaa90a7c1aXiamenCoreWallyPnkHndSntzrAlch70

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78868-00878868-008-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
FD&C RED NO. 4X3W0AM1JLXIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
WATER059QF0KO0RIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
D&C RED NO. 339DBA0SBB0LIACT
ALCOHOL3K9958V90MACTIB

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
2f357cbb-ccda-9f94-e063-6294a90a815bc0ab68ca-cdb6-3dc6-e053-2a95a90a00a32025-02-28WarningsExact identifier
spl set id: c0ab68ca-cdb6-3dc6-e053-2a95a90a00a3

Reported adverse events (FAERS/openFDA)#

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