FDA.reportPublic FDA data

SANIPRO DISINFECTANT WIPES

Manufacturer
AJ Co., Ltd.
Effective date
2020-08-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:25:13

Label at a glance#

ProductSANIPRO DISINFECTANT WIPES
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride

INACTIVE INGREDIENT SECTION

Propylene Glycol
Phenoxyethanol
Glycerin
Sodium Benzoate
Sodium Citrate
Disodium EDTA
Polysorbate 20
Citric Acid
Melaleuca Alternifolia (Tea Tree) Leaf Oil
Tocopheryl Acetate

OTC - PURPOSE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

Thoroughly wipe hands with wipe.

Discard properly. Not flushable.

Be sure to close lid to keep wipes moist.

WARNINGS SECTION

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

Do not use

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

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse 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.

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038856benzalkonium Cl 0.1 % Medicated PadPSN2
1038856benzalkonium chloride 1 MG/ML Medicated PadSCD2
1038856benzalkonium chloride 0.1 % Medicated WipesSY2
1038856benzalkonium chloride 0.1 % Topical SwabSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75356-0004-12025-01-30C16284748780-12cef2736-ada4-d83d-e063-dadaa90ab31fac55e43a-738f-49d2-e053-2a95a90a037f
75356-0004-22025-01-30C16284748780-12cef2736-ada4-d83d-e063-dadaa90ab31fac55e43a-738f-49d2-e053-2a95a90a037f

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75356-0004-1SANIPRO DISINFECTANT WIPES400 g in 1 PACKAGELIQUID4002
75356-0004-2SANIPRO DISINFECTANT WIPES80 g in 1 PACKAGELIQUID802

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75356-0004SANIPRO DISINFECTANT WIPES (BENZALKONIUM CHLORIDE) LIQUID [AJ CO., LTD.]2Legacy NDC, 2 package rows20200820_ac55e43a-738f-49d2-e053-2a95a90a037f.zip

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
75356-000475356-0004-1, 75356-0004-2

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
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
ad35fa25-0f01-37e1-e053-2a95a90ac6f4ac55e43a-738f-49d2-e053-2a95a90a037f2020-08-19WarningsExact identifier
spl id: ad35fa25-0f01-37e1-e053-2a95a90ac6f4
spl set id: ac55e43a-738f-49d2-e053-2a95a90a037f

Reported adverse events (FAERS/openFDA)#

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