FDA.reportPublic FDA data

Stride Products Hand Sanitizing Wipes

Manufacturer
Stride Engineering Inc.
Effective date
2021-02-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:54:08

Label at a glance#

ProductStride Products Hand Sanitizing Wipes
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Antiseptic (skin) cleanser. Effective in destroying (harmful) bacteria to provide antiseptic cleansing.

Dosage and administration

For occasional and personal domestic use by adults and children over 2 years. Supervise children when they use this product. Rub thoroughly into hands for at least 30 seconds and allow to dry.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol (Ethanol) 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic (skin) cleanser

Uses

INDICATIONS & USAGE SECTION

Antiseptic (skin) cleanser. Effective in destroying (harmful) bacteria to provide antiseptic cleansing.

Warnings

WARNINGS SECTION

For external use only. Flammable, keep away from open flame and sources of heat.

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

Stop use and ask/consult a doctor/physician/health care practitioner/health care provider/healthcare professional if irritation develops

Directions

DOSAGE & ADMINISTRATION SECTION

For occasional and personal domestic use by adults and children over 2 years. Supervise children when they use this product. Rub thoroughly into hands for at least 30 seconds and allow to dry.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, call a poison control center or get medical help right away.

Other information

SPL UNCLASSIFIED SECTION

This product is insoluble in water. Dispose of used wipes in trash, do not flush into toilet. This product may discolor certain fabrics or surfaces.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Propylene Glycol, Chlorphenesin, Disodium EDTA, Cetylpyridinium Chloride, Alkyl Polyglycoside.

Product labels

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

image descriptionimage description

image descriptionimage description

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
80752-00180752-001-01, 80752-001-02, 80752-001-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CHLORPHENESINI670DAL4SZIACT
EDETATE DISODIUM7FLD91C86KIACT
CETYLPYRIDINIUM CHLORIDED9OM4SK49PIACT
CAPRYL/CAPRYLYL MONO AND DIGLUCOSIDESEMV48HQP03IACT
ALCOHOL3K9958V90MACTIB

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
f1ed5507-5548-7ee3-e053-2995a90a771af08b2ea6-9045-42ae-8a54-3efa969e00c42023-01-10WarningsExact identifier
spl set id: f08b2ea6-9045-42ae-8a54-3efa969e00c4

Reported adverse events (FAERS/openFDA)#

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