FDA.reportPublic FDA data

Instant Hand Sanitizeing Wipe

Manufacturer
Shandong Yayun Sanitary Products Co., Ltd.
Effective date
2024-11-21
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 00:38:43

Label at a glance#

ProductInstant Hand Sanitizeing Wipe
Active ingredientPROPYLENE GLYCOL
Label structure13 sections

Dosage and administration

Wipe the surface of 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

Instant Hand Sanitizeing Wipe

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

BENZALKONIUM CHLORIDE 1.2g/pcs. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Instant Hand Sanitizeing Wipe

Use

INDICATIONS & USAGE SECTION

Instant Hand Sanitizeing Wipe 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 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

WATER
SODIUM CITRATE
Compound double-stranded quaternary ammonium salt

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

22

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79539-002-01Instant Hand Sanitizeing Wipe10 in 1 BAGCLOTH106
79539-002-02Instant Hand Sanitizeing Wipe20 in 1 BAGCLOTH206
79539-002-03Instant Hand Sanitizeing Wipe30 in 1 BAGCLOTH306
79539-002-04Instant Hand Sanitizeing Wipe40 in 1 BAGCLOTH406
79539-002-05Instant Hand Sanitizeing Wipe50 in 1 BAGCLOTH506
79539-002-06Instant Hand Sanitizeing Wipe60 in 1 BAGCLOTH606
79539-002-07Instant Hand Sanitizeing Wipe70 in 1 BAGCLOTH706
79539-002-08Instant Hand Sanitizeing Wipe80 in 1 BAGCLOTH806
79539-002-09Instant Hand Sanitizeing Wipe100 in 1 BAGCLOTH1006
79539-002-10Instant Hand Sanitizeing Wipe120 in 1 BAGCLOTH1206
79539-002-11Instant Hand Sanitizeing Wipe150 in 1 BAGCLOTH1506
79539-002-12Instant Hand Sanitizeing Wipe160 in 1 BAGCLOTH1606
79539-002-13Instant Hand Sanitizeing Wipe180 in 1 BAGCLOTH1806
79539-002-14Instant Hand Sanitizeing Wipe200 in 1 BAGCLOTH2006
79539-002-15Instant Hand Sanitizeing Wipe300 in 1 BAGCLOTH3006
79539-002-16Instant Hand Sanitizeing Wipe400 in 1 BAGCLOTH4006
79539-002-17Instant Hand Sanitizeing Wipe500 in 1 BAGCLOTH5006
79539-002-18Instant Hand Sanitizeing Wipe600 in 1 BAGCLOTH6006
79539-002-19Instant Hand Sanitizeing Wipe700 in 1 BAGCLOTH7006
79539-002-20Instant Hand Sanitizeing Wipe800 in 1 BAGCLOTH8006
79539-002-21Instant Hand Sanitizeing Wipe1000 in 1 BAGCLOTH10006
79539-002-22Instant Hand Sanitizeing Wipe1200 in 1 BAGCLOTH12006
79539-002-23Instant Hand Sanitizeing Wipe1600 in 1 BAGCLOTH16006
79539-002-24Instant Hand Sanitizeing Wipe2000 in 1 BAGCLOTH20006

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79539-002INSTANT HAND SANITIZEING WIPE (ISOPROPANOL AND COMPOUND DOUBLE-STRANDED QUATERNARY AMMONIUM SALTS) CLOTH [SHANDONG YAYUN SANITARY PRODUCTS CO., LTD.]6Current NDC, 24 package rows20241123_aa0dc01a-2c6b-7402-e053-2a95a90af6a2.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79539-00279539-002-01, 79539-002-02, 79539-002-03, 79539-002-04, 79539-002-05, 79539-002-06, 79539-002-07, 79539-002-08, 79539-002-09, 79539-002-10, 79539-002-11, 79539-002-12, 79539-002-13, 79539-002-14, 79539-002-15, 79539-002-16, 79539-002-17, 79539-002-18, 79539-002-19, 79539-002-20, 79539-002-21, 79539-002-22, 79539-002-23, 79539-002-24

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
ALOE BARBADENSIS LEAF EXTRACTZY81Z83H0XIACT
EDETATE DISODIUM7FLD91C86KIACT
PROPYLENE GLYCOL6DC9Q167V3ACTIB
PHENOXYETHANOLHIE492ZZ3TIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
WATER059QF0KO0RIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
CETYLPYRIDINIUM CHLORIDED9OM4SK49PIACT
SULFURYL FLUORIDE64B59K7U6QIACT
SODIUM CITRATE1Q73Q2JULRIACT
CHAMOMILEFGL3685T2XIACT

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 WipeISOPROPANOL AND COMPOUND DOUBLE-STRANDED QUATERNARY AMMONIUM SALTSShandong Yayun Sanitary Products Co., Ltd.aa0dc01a-2c6b-7402-e053-2a95a90af6a22024-11-21WarningsExact identifier
ndc (package): 79539-002-17
ndc (package): 79539-002-08
ndc (package): 79539-002-22
ndc (package): 79539-002-16
ndc (package): 79539-002-19
ndc (package): 79539-002-06
ndc (package): 79539-002-20
ndc (package): 79539-002-05
ndc (package): 79539-002-03
ndc (package): 79539-002-12
ndc (package): 79539-002-23
ndc (package): 79539-002-18
ndc (package): 79539-002-09
ndc (package): 79539-002-15
ndc (package): 79539-002-24
ndc (package): 79539-002-07
ndc (package): 79539-002-13
ndc (package): 79539-002-21
ndc (package): 79539-002-02
ndc (package): 79539-002-10
ndc (package): 79539-002-04
ndc (package): 79539-002-11
ndc (package): 79539-002-14
ndc (package): 79539-002-01
ndc (product): 79539-002
ndc11 (package): 79539000224
ndc11 (package): 79539000221
ndc11 (package): 79539000212
ndc11 (package): 79539000201
ndc11 (package): 79539000205
ndc11 (package): 79539000208
ndc11 (package): 79539000219
ndc11 (package): 79539000209
ndc11 (package): 79539000218
ndc11 (package): 79539000223
ndc11 (package): 79539000216
ndc11 (package): 79539000202
ndc11 (package): 79539000213
ndc11 (package): 79539000220
ndc11 (package): 79539000214
ndc11 (package): 79539000215
ndc11 (package): 79539000222
ndc11 (package): 79539000211
ndc11 (package): 79539000204
ndc11 (package): 79539000210
ndc11 (package): 79539000207
ndc11 (package): 79539000206
ndc11 (package): 79539000203
ndc11 (package): 79539000217
spl id: 2778cad1-2929-fab8-e063-6294a90a2fc7
spl set id: aa0dc01a-2c6b-7402-e053-2a95a90af6a2

Reported adverse events (FAERS/openFDA)#

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