FDA.reportPublic FDA data

ANTI BYE HAND SANITIZER WIPES

Manufacturer
Perfumeholic Inc
Effective date
2020-09-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:13:57

Label at a glance#

ProductANTI BYE HAND SANITIZER WIPES
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Hand sanitizer to help reduce bacteria that potentially can cause disease.

Dosage and administration

• Place enough product on hands to cover all surfaces. Rub hands together until dry. • Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ALCOHOL 70% w/w

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Sodium benzoate, PEG-60 hydrogenated castor oil, Lavandula Angustifolia (Lavender) Oil, Butylene Glycol, Aloe Vera Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract

PURPOSE

OTC - PURPOSE SECTION

Antibacterial

WARNINGS

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

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Do not use
• in children less than 2 months of age
• on open skin wounds
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When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
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Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease.

Directions

DOSAGE & ADMINISTRATION SECTION

• Place enough product on hands to cover all surfaces. Rub hands together until dry.

• Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

OTHER SAFETY INFORMATION

• Store between 15-30C (59-86F)

• Avoid freezing and excessive heat above 40C (104F)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of containerImage of container

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
75773-06075773-060-01

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
WATER059QF0KO0RIACT
SODIUM BENZOATEOJ245FE5EUIACT
PEG-60 HYDROGENATED CASTOR OIL02NG325BQGIACT
LAVENDER OILZBP1YXW0H8IACT
BUTYLENE GLYCOL3XUS85K0RAIACT
ALOE VERA LEAFZY81Z83H0XIACT
CHAMOMILEFGL3685T2XIACT
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
dce83c11-5a7c-0fd4-e053-2995a90a7ab858e6ca59-52b0-4ff5-b4ae-a47ebcc92d442022-04-18WarningsExact identifier
spl set id: 58e6ca59-52b0-4ff5-b4ae-a47ebcc92d44

Reported adverse events (FAERS/openFDA)#

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