FDA.reportPublic FDA data

Diva Protect Antibacterial Hand Cleanser

Manufacturer
Diva International Inc.
Effective date
2022-02-18
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:08:23

Label at a glance#

ProductDiva Protect Antibacterial Hand Cleanser
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

Antibacterial Hand Cleanser. Effective in destroying harmful bacteria to provide antiseptic cleansing.

Dosage and administration

Adults and children over 2 years: For occasional and personal domestic use. Supervise children when they use this product Lather in hands with water for at least 30 seconds rinse well.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride   0.15%

Purpose

OTC - PURPOSE SECTION

Antibacterial Hand Cleanser

Uses

INDICATIONS & USAGE SECTION

Antibacterial Hand Cleanser. Effective in destroying harmful bacteria to provide antiseptic cleansing.

Warnings

WARNINGS SECTION

  • For external use only.
  • When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.
  • Stop use and ask a doctor if irritation develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children over 2 years:

  • For occasional and personal domestic use.
  • Supervise children when they use this product
  • Lather in hands with water for at least 30 seconds rinse well.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Cocamidopropyl Betaine, Glycerin,  Lauramine oxide, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Matricaria recutita (Chamomile) Extract, Tetrasodium EDTA, Methylchloroisothiazolinone (and) Methylisothiazolinone, Parfum, Citric Acid

Other Information

SPL UNCLASSIFIED SECTION

Do not use on your Divacup

Questions?

Consumer care : 1-866-444-3482

support@divacup.com

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77116-00377116-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
GLYCERINPDC6A3C0OXIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
EDETATE SODIUMMP1J8420LUIACT
METHYLCHLOROISOTHIAZOLINONE/METHYLISOTHIAZOLINONE MIXTURE15O9QS218WIACT
LAURAMINE OXIDE4F6FC4MI8WIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALOE VERA LEAFZY81Z83H0XIACT
CHAMOMILEFGL3685T2XIACT
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
d84ade9f-0aa4-0ba9-e053-2a95a90a42bf7e0271b8-e19f-4c68-bf67-958e7c2f1e152022-02-18WarningsExact identifier
spl id: d84ade9f-0aa4-0ba9-e053-2a95a90a42bf
spl set id: 7e0271b8-e19f-4c68-bf67-958e7c2f1e15

Reported adverse events (FAERS/openFDA)#

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