Walter 70% Alcohol Hand Sanitizer Wipes

Manufacturer
Walter Surface Technologies Inc. | Walter Surface Technologies, inc.
Effective date
2022-01-19
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:11:49

Label at a glance#

ProductWalter 70% Alcohol Hand Sanitizer Wipes
Active ingredientALCOHOL
Label structure9 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Alcohol 70%

OTC - PURPOSE SECTION

Purpose
Antiseptic

INDICATIONS & USAGE SECTION

Uses

to decrease bacteria on the skin

WARNINGS SECTION

Warnings
For external use only.

Flammable. Keep away from fire or flame.

OTC - WHEN USING SECTION

When using this product keep away from eyes. In case of eye contact, rinse eyes with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develop or last more than 72 hours.

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.

DOSAGE & ADMINISTRATION SECTION

Directions

  • rub wipe thoroughly over all surfaces of both hands and allow to dry.
  • supervise children under 6 years old
  • not recommended for infants

INACTIVE INGREDIENT SECTION

Inactive ingredients

water (aqua), glycerin, propylene glycol, isopropyl myristate, dl-alpha tocopherol acetate, denatonium benzoate

SPL UNCLASSIFIED SECTION

QUESTIONS? USA 1-866-592-5837
walter.com
WALTER
Manufactured by: Walter Surface Technologies Inc.
5977 Trans Canada Highway, Pointe Claire
Quebec H9R 1C1 CANADA
MADE IN CANADA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

WALTER
KILLS HARMFUL BACTERIA
Fragrance Free
70% ALCOHOL
HAND SANITIZER WIPES

400 Wipes (5.5 in. x 8 in. / 13.8 cm x 20.3 cm)

USA_HS_WIPES_400USA_HS_WIPES_400

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
77621-00377621-003-09, 77621-003-10, 77621-003-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
d66fc9cd-c98b-a62e-e053-2a95a90a33dab3d51934-d3f6-37d0-e053-2a95a90ab0c22022-01-19WarningsExact identifier
spl id: d66fc9cd-c98b-a62e-e053-2a95a90a33da
spl set id: b3d51934-d3f6-37d0-e053-2a95a90ab0c2

Reported adverse events (FAERS/openFDA)#

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