FDA.reportPublic FDA data

Clearly Better by Intercom Alcohol-Free Hand Sanitizer

Manufacturer
Dyno Manufacturing
Effective date
2021-03-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:48:20

Label at a glance#

ProductClearly Better by Intercom Alcohol-Free Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

For hand washing to help reduce bacteria on the skin For use when soap is not available

Dosage and administration

Pump a small amount of foam into palm of hand Rub thoroughly over all surfaces of both hands Rub hands together briskly until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

  • For hand washing to help reduce bacteria on the skin
  • For use when soap is not available

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

Avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or redness develops, or 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

  • Pump a small amount of foam into palm of hand
  • Rub thoroughly over all surfaces of both hands
  • Rub hands together briskly until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Cocamidopropyl PG-Dimonium Chloride Phosphate, dihyrdroxyethyl cocamine oxide, acetamidoethoxyethanol, citric acid, Fragrance

Clearly Better by Intercom Alcohol-Free Hand Sanitizer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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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
79532-01379532-013-34

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATEH2KVQ74JM4IACT
DIHYDROXYETHYL COCAMINE OXIDE8AR51R3BL5IACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
ACETAMIDOETHOXYETHANOLLVX2APC4XRIACT

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
bec2e70d-8cfc-69e5-e053-2995a90ad6f9bec2dde1-70bf-5c04-e053-2a95a90a6daf2021-03-30WarningsExact identifier
spl id: bec2e70d-8cfc-69e5-e053-2995a90ad6f9
spl set id: bec2dde1-70bf-5c04-e053-2a95a90a6daf

Reported adverse events (FAERS/openFDA)#

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