FDA.reportPublic FDA data

B4 HAND SANITIZER ALCOHOL-FREE

Manufacturer
Ming Fai Industrial (Shenzhen) Co. Ltd
Effective date
2019-11-29
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
legacy-cache
Hydrated at
2026-08-01 23:55:40

Label at a glance#

ProductB4 HAND SANITIZER ALCOHOL-FREE
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

For handwashing to decrease bacteria on the skin.

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping.

Label contents#

Full prescribing information#

DRUG FACTS ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

BENZALKONIUM CHLORIDE 0.13%

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

USES

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on the skin.

WARNINGS

WARNINGS SECTION

For external use only.

DO NOT USE

OTC - DO NOT USE SECTION

in the eyes

Stop use and ask a doctor if:

  • irritation and redness develop
  • if condition persists for more than 72 hours

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping.

OTHER INFORMATION

OTHER SAFETY INFORMATION

store at room temperature

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Butylene Glycol, Glycerin, Caeesolpinia Spinosa Gum, Fragrance Sodium Lauryl Sulfate, Ethylhexylglycerin, Phenoxyethanol

DISTRIBUTED BY

SPL UNCLASSIFIED SECTION

Midway Advanced Products, LLC

Houston, TX 77024

888.238.9284 | b4products.com

Made In China

PRODUCT LABELING

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabelPacket label and drug factsPacket label and drug facts

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
56153-40056153-400-07, 56153-400-27

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CAESALPINIA SPINOSA RESINWL3883U2POIACT
GLYCERINPDC6A3C0OXIACT
SODIUM LAURYL SULFATE368GB5141JIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
PHENOXYETHANOLHIE492ZZ3TIACT
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
b815146f-65ad-6e92-e053-2995a90a7c2e357b2e82-b6aa-22c6-e054-00144ff8d46c2021-01-04WarningsExact identifier
spl set id: 357b2e82-b6aa-22c6-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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