Alcohol Wet Wipes, 70 Alcohol

Manufacturer
Sweda Company LLC
Effective date
2020-08-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:18:03

Label at a glance#

ProductAlcohol Wet Wipes, 70 Alcohol
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

For hand-washing to decrease bacteria on the skin

Dosage and administration

Slowly peel back label and use one wipe. Reseal, keep closed to prevent evaporation. Thoroughly wipe hands, allow to dry out rinsing. Discard after single use  

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol(70.00% V/V)

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • For hand-washing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

Flammable. Keep away from heat and flame.

For External use only

Do not use

OTC - DO NOT USE SECTION

in eyes. In case of contact, rinse thoroughly with water.

Stop use & ask doctor

OTC - STOP USE SECTION

if rash/redness or irritation appears/develops and persists for more than 72 hours.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

except under adult supervision. If swallowed, get medical help or contact a Poison Control Center

Directions

DOSAGE & ADMINISTRATION SECTION

  • Slowly peel back label and use one wipe. Reseal, keep closed to prevent evaporation.
  • Thoroughly wipe hands, allow to dry out rinsing. Discard after single use  

Other information

SPL UNCLASSIFIED SECTION

  • Do not flush down toilet.
  • Keep away from sunlight.Store at room temperature 20°-25°Celsius (68°-77° Fahrenheit)
  • May discolor certain fabrics

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aqua, Glycerin, Aloe Barbadensis Leaf Juice, D- Panthenol, Phenoxyethanol

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
90121-00190121-001-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
bb61c361-fd3a-1748-e053-2995a90a7153ad53cd9a-64fb-9af3-e053-2995a90ae15d2021-02-15WarningsExact identifier
spl set id: ad53cd9a-64fb-9af3-e053-2995a90ae15d

Reported adverse events (FAERS/openFDA)#

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