FDA.reportPublic FDA data

Be Safe Sanitizing Wipes

Manufacturer
Reliance Global Trading | Hangzhou Caring Cleaning Commodity Co., Ltd
Effective date
2020-06-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:16:19

Label at a glance#

ProductBe Safe Sanitizing Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

Antiseptic

OTC - PURPOSE SECTION

hand sanitizer to help reduce bacteria on skin

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

INDICATIONS & USAGE SECTION

to decrease bacteria on the skin

WARNINGS SECTION

For external hands only

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center right away.

INACTIVE INGREDIENT SECTION

water, glycerin, polysorbate 20, aloe leaf extract, chamomilla flower extract, sodium benzoate, phenoxethanol, tocopheryl acetate, citric acid

INSTRUCTIONS FOR USE SECTION

wipe hands thoroughly with product and allow to dry

keep out of eyes. In case of contact with eyes, flush thoroughly with water.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78249-100-012022-01-28C16284748780-1d6a99b39-a7db-a426-e053-dadaa90af4c2Be Safe Sanitizing Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78249-100-01Be Safe Sanitizing Wipes100 in 1 CANISTERCLOTH1002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78249-100BE SAFE SANITIZING WIPES CLOTH [RELIANCE GLOBAL TRADING]2Legacy NDC, 1 package rows20200606_ecaf32bc-f56f-4028-a7ac-fc091a33a63d.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78249-10078249-100-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
POLYSORBATE 207T1F30V5YHIACT
ALOE VERA LEAFZY81Z83H0XIACT
CHAMOMILE FLOWER OIL60F80Z61A9IACT
SODIUM BENZOATEOJ245FE5EUIACT
PHENOXYETHANOLHIE492ZZ3TIACT
TOCOPHEROLR0ZB2556P8IACT
CITRIC ACID ACETATEDSO12WL7AUIACT
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
a74c92e0-74be-4943-e053-2995a90ae2cfecaf32bc-f56f-4028-a7ac-fc091a33a63d2020-06-04WarningsExact identifier
spl id: a74c92e0-74be-4943-e053-2995a90ae2cf
spl set id: ecaf32bc-f56f-4028-a7ac-fc091a33a63d

Reported adverse events (FAERS/openFDA)#

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