Instant Hand Sanitizeing Wipe

Manufacturer
SHANDONG HENGFA HYGIENIC PRODUCTS CO., LTD.
Effective date
2026-01-08
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:32:10

Label at a glance#

ProductInstant Hand Sanitizeing Wipe
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

Wipe the surface of the skin

Storage and handling

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

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Instant Hand Sanitizeing Wipe

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 1mL/pcs. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

To help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wipe the surface of the skin

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
HYDROGEN PEROXIDE

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79913-201-01Instant Hand Sanitizeing Wipe1 in 1 BAGCLOTH14
79913-201-02Instant Hand Sanitizeing Wipe12 in 1 BAGCLOTH124
79913-201-03Instant Hand Sanitizeing Wipe40 in 1 BAGCLOTH404
79913-201-04Instant Hand Sanitizeing Wipe80 in 1 BAGCLOTH804
79913-201-05Instant Hand Sanitizeing Wipe100 in 1 BAGCLOTH1004
79913-201-06Instant Hand Sanitizeing Wipe135 in 1 PAILCLOTH1354

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79913-20179913-201-01, 79913-201-02, 79913-201-03, 79913-201-04, 79913-201-05, 79913-201-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
HYDROGEN PEROXIDEBBX060AN9VIACT
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
Instant Hand Sanitizeing WipeALCOHOLSHANDONG HENGFA HYGIENIC PRODUCTS CO., LTD.bd17c0c7-d824-6b03-e053-2995a90afe152026-01-08WarningsExact identifier
ndc (package): 79913-201-01
ndc (package): 79913-201-02
ndc (package): 79913-201-04
ndc (package): 79913-201-03
ndc (package): 79913-201-06
ndc (package): 79913-201-05
ndc (product): 79913-201
ndc11 (package): 79913020104
ndc11 (package): 79913020105
ndc11 (package): 79913020101
ndc11 (package): 79913020102
ndc11 (package): 79913020106
ndc11 (package): 79913020103
spl id: 47dbe477-9d00-35a6-e063-6294a90ab6cc
spl set id: bd17c0c7-d824-6b03-e053-2995a90afe15

Reported adverse events (FAERS/openFDA)#

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