FDA.reportPublic FDA data

ATOREN ANTIBACTERIAL WIPES

Manufacturer
MLS
Effective date
2020-07-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:22:44

Label at a glance#

ProductATOREN ANTIBACTERIAL WIPES
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Adults and children over 2 years old: For occasional and personal domestic use. Supervise children when they use this product. Rub thoroughly into hands for at least 30 seconds. Allow to dry.

Storage and handling

Store between 15-30C (59-86F). Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

USE

DOSAGE & ADMINISTRATION SECTION

Decreases bacteria on skin.

WARNINGS

WARNINGS SECTION

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

WARNINGS

OTC - WHEN USING SECTION

Avoid contact with eyes. If contact occurs, rinse thoroughly with water.

WARNINGS

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if irritation develops.

WARNINGS

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, call a poison control center or get medical help right away.

DIRECTIONS

INDICATIONS & USAGE SECTION

Adults and children over 2 years old: For occasional and personal domestic use. Supervise children when they use this product. Rub thoroughly into hands for at least 30 seconds. Allow to dry.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

Store between 15-30C (59-86F). Avoid freezing and excessive heat above 40C (104F)

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Citric Acid, Sodium Citrate, Butylene Glycol

DO NOT USE

OTC - DO NOT USE SECTION

if you are allergic to any of the ingredients.

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

190g NDC: 73984-334-01 Label190g NDC: 73984-334-01 Label

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73984-33473984-334-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
SODIUM CITRATE1Q73Q2JULRIACT
BUTYLENE GLYCOL3XUS85K0RAIACT

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
b937cf6a-0837-9136-e053-2a95a90ad07ca9ed2712-dbe4-3deb-e053-2995a90a0ca32021-01-18WarningsExact identifier
spl set id: a9ed2712-dbe4-3deb-e053-2995a90a0ca3

Reported adverse events (FAERS/openFDA)#

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