FDA.reportPublic FDA data

Alcohol sanitizer wipes

Manufacturer
SHANDONG HENGFA HYGIENIC PRODUCTS CO., LTD.
Effective date
2025-12-19
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:26:54

Label at a glance#

ProductAlcohol sanitizer wipes
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

Wipe the skin and let it dry naturally Supervise children under 6 years of age when using this product to avoid swallowing.

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

Alcohol sanitizer wipes

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 1mL/pcs. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Alcohol sanitizer wipes

Use

INDICATIONS & USAGE SECTION

Alcohol sanitizer wipes 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 skin and let it dry naturally
  • Supervise children under 6 years of age when using this product to avoid swallowing.

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

hydrogen peroxide, purified water USP

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79913-101-01Alcohol sanitizer wipes1 in 1 BAGCLOTH14
79913-101-02Alcohol sanitizer wipes10 in 1 BAGCLOTH104
79913-101-03Alcohol sanitizer wipes40 in 1 BAGCLOTH404
79913-101-04Alcohol sanitizer wipes50 in 1 BAGCLOTH504
79913-101-05Alcohol sanitizer wipes80 in 1 BAGCLOTH804
79913-101-06Alcohol sanitizer wipes100 in 1 BAGCLOTH1004

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79913-10179913-101-01, 79913-101-02, 79913-101-03, 79913-101-04, 79913-101-05, 79913-101-06

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
HYDROGEN PEROXIDEBBX060AN9VIACT
WATER059QF0KO0RIACT
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
Alcohol sanitizer wipesALCOHOL/PURIFIED WATERSHANDONG HENGFA HYGIENIC PRODUCTS CO., LTD.ab9634bd-4226-2f73-e053-2995a90a802f2025-12-19WarningsExact identifier
ndc (package): 79913-101-03
ndc (package): 79913-101-05
ndc (package): 79913-101-01
ndc (package): 79913-101-04
ndc (package): 79913-101-06
ndc (package): 79913-101-02
ndc (product): 79913-101
ndc11 (package): 79913010106
ndc11 (package): 79913010103
ndc11 (package): 79913010102
ndc11 (package): 79913010104
ndc11 (package): 79913010101
ndc11 (package): 79913010105
spl id: 464a703c-52f0-81ff-e063-6294a90a84c9
spl set id: ab9634bd-4226-2f73-e053-2995a90a802f

Reported adverse events (FAERS/openFDA)#

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