WIPESPLUS HAND SANITIZING WIPES

Manufacturer
CFS Brands
Effective date
2025-04-21
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:07:21

Label at a glance#

ProductWIPESPLUS HAND SANITIZING WIPES
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

Directions - rub wipe thoroughly over all surfaces of both hands - allow to dry without wiping - supervise children under 6 years old - not recommended for infants - dispose of wipe in trash; do not flush

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient alcohol 70%

OTC - PURPOSE SECTION

Purpose antiseptic

INDICATIONS & USAGE SECTION

Use For hand sanitizing to decrease bacteria on the skin.

WARNINGS SECTION

Warnings

for external use only.

Flammable, keep away from flame or heat

OTC - DO NOT USE SECTION

Do not use in or contact with eyes

OTC - STOP USE SECTION

Stop use and ask a doctor • if redness or irritation develops

• If conditions persist for more than 72 hours, consult a physician

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children unless under adult supervision.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions
- rub wipe thoroughly over all surfaces of both hands
- allow to dry without wiping
- supervise children under 6 years old
- not recommended for infants
- dispose of wipe in trash; do not flush

INACTIVE INGREDIENT SECTION

Inactive ingredient: water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hand sanitizing wipe alcohol freeHand sanitizing wipe alcohol free

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797544isopropyl alcohol 70 % Medicated PadPSN3
797544isopropyl alcohol 0.7 ML/ML Medicated PadSCD3
797544isopropyl alcohol 70 % Medicated PadSY3
797544isopropyl alcohol 70 % Topical ClothSY3
797544isopropyl alcohol 70 % Topical SwabSY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84376-001-01WIPESPLUS HAND SANITIZING WIPES100 in 1 POUCHCLOTH1003
84376-001-02WIPESPLUS HAND SANITIZING WIPES200 in 1 POUCHCLOTH2003
84376-001-03WIPESPLUS HAND SANITIZING WIPES240 in 1 CANISTERCLOTH2403

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84376-00184376-001-01, 84376-001-02, 84376-001-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT

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
WIPESPLUS HAND SANITIZING WIPESALCOHOLCFS Brands396e1b0a-1a0e-7dd0-e063-6394a90a67b02025-04-21WarningsExact identifier
ndc (package): 84376-001-03
ndc (package): 84376-001-02
ndc (package): 84376-001-01
ndc (product): 84376-001
ndc11 (package): 84376000101
ndc11 (package): 84376000102
ndc11 (package): 84376000103
spl id: 334f6cb4-e898-d337-e063-6394a90ae604
spl set id: 396e1b0a-1a0e-7dd0-e063-6394a90a67b0

Reported adverse events (FAERS/openFDA)#

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