ANTI BYE ETHANOL 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 ETHANOL WIPES
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

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

Dosage and administration

Directions: • 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

Active ingredients: ALCOHOL 75% w/w

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

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

Purpose: Antibacterial

WARNINGS

WARNINGS SECTION

Warnings:

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

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Uses

INDICATIONS & USAGE SECTION

Uses:

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

Directions

DOSAGE & ADMINISTRATION SECTION

Directions:

• 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

Other 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
75773-02075773-020-01

Ingredients#

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

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

Source Document#

Source XML · Source PDF

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
dce83c11-5a7a-0fd4-e053-2995a90a7ab816c5cd75-08b3-4fe2-bc62-41479f0ddfc62022-04-18WarningsExact identifier
spl set id: 16c5cd75-08b3-4fe2-bc62-41479f0ddfc6

Reported adverse events (FAERS/openFDA)#

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