FDA.reportPublic FDA data

Mova Liquid Hand Antibacterial

Manufacturer
Mova Chemical S.A
Effective date
2023-01-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:52:57

Label at a glance#

ProductMova Liquid Hand Antibacterial
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Dosage and administration

Wet hands with water-lather vigorously and wash skin-rinse and dry thoroughly. For home and institutional use

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Antiseptic liquid hand soap to help decrease bacteria on the skin.
Recommended for repeated use.

Warnings

WARNINGS SECTION

  • Allergy alert DOES NOT contain essential almond oil.

Do not use

OTC - DO NOT USE SECTION

  • on intimate parts of the body.
  • Use for hand washing only.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Avoid contact with eyes. In case of eye contact, flush with water. If swallowed, get medical help or contact a Poison Control Center.

Directions for use

DOSAGE & ADMINISTRATION SECTION

  • Wet hands with water-lather vigorously and wash skin-rinse and dry thoroughly.
  • For home and institutional use

Other Information

SPL UNCLASSIFIED SECTION

  • Store at room temperature no higher than 45°C (113°F) Avoid direct sunlight.
  • Keep in closed containers, free from direct sunlight.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Triethanolamine (TEA), Glycerin USP, Probethaine PB-12, Methylether PPG-2, Methylisothiazoline, Tetrasodium EDTA, Citric Acid, Almond Fragrance, Glycol Distearate.

Question or Coments?

OTC - QUESTIONS SECTION

  • Call USA +512-853-9176 Monday through Friday 8:00am to 4:30pm CST.
  • Call Panama +507 831-1181 Monday through Friday 8:00am to 4:30pm CST.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81235-001-012024-07-30C16284748780-11030e365-2827-111a-e063-dadaa90a10e2Mova Liquid Hand Soap Antibacterial
81235-001-012024-01-30C16284748780-11030e365-2827-111a-e063-dadaa90a10e2Mova Liquid Hand Soap Antibacterial

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81235-001-01Mova Liquid Hand Antibacterial3785 mL in 1 BOTTLEGEL37852

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81235-001MOVA LIQUID HAND ANTIBACTERIAL (BENZALKONIUM CHLORIDE) GEL [MOVA CHEMICAL S.A]2Legacy NDC, 1 package rows20230106_b70fa3e1-85a7-3174-e053-2a95a90a2205.zip

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
81235-00181235-001-01

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
TROLAMINE9O3K93S3TKIACT
GLYCERINPDC6A3C0OXIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
EDETATE SODIUMMP1J8420LUIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
GLYCOL DISTEARATE13W7MDN21WIACT
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
f17d6854-cc0f-2900-e053-2a95a90a3ab0b70fa3e1-85a7-3174-e053-2a95a90a22052023-01-04WarningsExact identifier
spl id: f17d6854-cc0f-2900-e053-2a95a90a3ab0
spl set id: b70fa3e1-85a7-3174-e053-2a95a90a2205

Reported adverse events (FAERS/openFDA)#

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