WIPE OUT Safe Pack

Manufacturer
TZUMI INNOVATIONS LLC | Shenzhen Meiya Display Co., Ltd. | Shenzhen Lantern Science Co., ltd. | FuYang YangYang Health Technology Co. Ltd
Effective date
2021-01-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:37:00

Label at a glance#

ProductWIPE OUT Safe Pack
Active ingredientALCOHOL, BENZALKONIUM CHLORIDE
Label structure21 sections

Indications and uses

Decreases bacteria and germs on the skin that could cause disease

Dosage and administration

Take a palmful of product in one hand, spread on both hands and rub into skin

Storage and handling

Do not store above 105F May discolor some fabrics Harmful to wood finishes and plastics

Label contents#

Full prescribing information#

WIPE OUT Hand Sanitizer with Moisturizers

SPL UNCLASSIFIED SECTION

WIPE OUT Hand Sanitizer with Moisturizers

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

■ To decrease bacteria on the skin

WARNINGS

WARNINGS SECTION

For external use only

Flammable. Keep away from fire or flame

When using this product, avoid contact with eyes
If contact occurs, rinse eyes thoroughly with water

Stop Use

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours

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

Directions

DOSAGE & ADMINISTRATION SECTION

Take a palmful of product in one hand, spread on both hands and rub into skin

Other information

STORAGE AND HANDLING SECTION

Do not store above 105F

May discolor some fabrics

Harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Aloe Barbadensis Leaf Extract, AMINOMETHYL PROPANOL, ACRYLATES/C10-30 ALKYL ACRYLATE
CROSSPOLYMER

WIPE OUT Antibacterial Wipes Travel Pack Lemon Scent

SPL UNCLASSIFIED SECTION

WIPE OUT Antibacterial Wipes Travel Pack Lemon Scent

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

Decreases bacteria and germs on the skin that could cause disease

Warnings

WARNINGS SECTION

For external use only

When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water.

Avoid contact with broken skin

Stop Use

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develop, condition persists for more than 72 hours

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 immediately

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping

For children under 6, use only under adult supervision

Not recommended for infants

Other Information

STORAGE AND HANDLING SECTION

Keep containers tightly closed in a dry, cool and well ventilated place
Recommended storage temperature: 32F to 104F (0C to 40C)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Fragrance, Water, Phenoxyethanol, Polysorbate 20, Propylene Glycol, Tocopheryl Acetate

Hand sanitizer label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Wipe label 1

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Wipe label 2

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Kit label 1

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Kit label 2

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1047755ethanol 75 % Topical SolutionPSN2
1047755ethanol 0.75 ML/ML Topical SolutionSCD2
1047755ethanol 75 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77878-014-012022-07-29C16284748780-1e4f33bdf-aa7f-d8a0-e053-dadaa90a6e4e77878-012, 013, 014, Wipe Out! Safe Pack (style# 7686HD)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77878-012-01WIPE OUT Safe Pack50 mL in 1 BOTTLESOLUTION50 mL75 mL in 100mL2
77878-013-01WIPE OUT Safe Pack10 in 1 PACKETSOLUTION106.8 mg2
77878-014-01WIPE OUT Safe Pack1 in 1 KITKIT12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77878-012WIPE OUT SAFE PACK (ALCOHOL, BENZALKONIUM CHLORIDE) KIT [TZUMI INNOVATIONS LLC]2Unmatched20210116_dfdf9d44-98bb-4664-90d7-35b393fc1795.zip
77878-013WIPE OUT SAFE PACK (ALCOHOL, BENZALKONIUM CHLORIDE) KIT [TZUMI INNOVATIONS LLC]2Unmatched20210116_dfdf9d44-98bb-4664-90d7-35b393fc1795.zip
77878-014WIPE OUT SAFE PACK (ALCOHOL, BENZALKONIUM CHLORIDE) KIT [TZUMI INNOVATIONS LLC]2Legacy NDC, 3 package rows20210116_dfdf9d44-98bb-4664-90d7-35b393fc1795.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77878-01477878-014-01
77878-01277878-012-01
77878-01377878-013-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
b8f265be-6d65-ed39-e053-2995a90ad179dfdf9d44-98bb-4664-90d7-35b393fc17952021-01-15WarningsExact identifier
spl id: b8f265be-6d65-ed39-e053-2995a90ad179
spl set id: dfdf9d44-98bb-4664-90d7-35b393fc1795

Reported adverse events (FAERS/openFDA)#

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