Sanitizerx Sanitizing Wipes

Manufacturer: Flash Sales Inc. | Fustin (Xiamen) Commodity Co., ltd
Effective date: 2020-07-21
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 23:20:40

Label at a glance#

ProductSanitizerx Sanitizing Wipes

Active ingredientALCOHOL

Label structure10 sections

Dosage and administration

For use apply thoroughly to hands and skin as desired. Discard wipe in trash receptacle after use. Do not flush. Keep the package opening securely shut to prevent the wipes from drying out.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

75% Ethyl Alcohol

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand cleansing to decrease bacteria on the hands, arms and legs.

Warnings

WARNINGS SECTION

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

OTC - WHEN USING SECTION

Keep out of eyes, ears, and mouth. In case of contact with eyes, rinse thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

For use apply thoroughly to hands and skin as desired. Discard wipe in trash receptacle after use. Do not flush. Keep the package opening securely shut to prevent the wipes from drying out.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water, Aloe vera extract, honeysuckle extract, Nonwoven fiber

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front and Back Labels50 wipes NDC: 77994-013-02

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

Sanitizerx Sanitizing Wipes
ALCOHOL
ALOE VERA LEAF
WATER
LONICERA JAPONICA FLOWER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
77944-013	77944-013-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALOE VERA LEAF	ZY81Z83H0X	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB
LONICERA JAPONICA FLOWER	4465L2WS4Y	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
c19fa026-3f92-f029-e053-2a95a90a1463			aafaf562-473e-0ce3-e053-2995a90a95b3	2021-05-05	Warnings	Exact identifier spl set id: aafaf562-473e-0ce3-e053-2995a90a95b3

Reported adverse events (FAERS/openFDA)#

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