FDA.reportPublic FDA data

Antiseptic Hand Sanitizer Alcohol Free Valencia Group

Manufacturer
Midway Advanced Products, LLC
Effective date
2018-07-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:53:31

Label at a glance#

ProductAntiseptic Hand Sanitizer Alcohol Free Valencia Group
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Dosage and administration

wet hands thoroughly with product allow to dry without wiping

Storage and handling

store at room temperature

Label contents#

Full prescribing information#

​Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%

​Purpose

OTC - PURPOSE SECTION

Antiseptic

​Use

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

OTC - STOP USE SECTION

  • irritation and redness develop
  • 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
  • allow to dry without wiping

​Other information

STORAGE AND HANDLING SECTION

  • store at room temperature

Hand Sanitizer 0.7mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SachetSachet

Hand Sanitizer 100 mL x 100 Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CartonCarton

Hand sanitizer 100 mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Hand Sanitizer Valencia

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

52490-501-23 Label52490-501-23 Label

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52490-50152490-501-03, 52490-501-22, 52490-501-40, 52490-501-23

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
BUTYLENE GLYCOL3XUS85K0RAIACT
CAESALPINIA SPINOSA RESINWL3883U2POIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
GLYCERINPDC6A3C0OXIACT
PHENOXYETHANOLHIE492ZZ3TIACT
SODIUM LAURYL SULFATE368GB5141JIACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

Source Document#

Source XML · Source PDF

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
70ba379a-6e2f-48c1-e053-2991aa0ae4f504893caa-24d4-488d-bea8-974d8dc80bd32018-07-11WarningsExact identifier
spl id: 70ba379a-6e2f-48c1-e053-2991aa0ae4f5
spl set id: 04893caa-24d4-488d-bea8-974d8dc80bd3

Reported adverse events (FAERS/openFDA)#

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