safeHands

Manufacturer
Safehands Solutions | National Pharma LLC
Effective date
2020-09-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:15:43

Label at a glance#

ProductsafeHands
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Dosage and administration

Liberally apply product to skin by gently massaging until absorbed. Supervise children in the use of the product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

  • To decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only.

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.

Do not use in eyes.

OTC - DO NOT USE SECTION

In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

skin/eye irritation develops.

Directions

DOSAGE & ADMINISTRATION SECTION

Liberally apply product to skin by gently massaging until absorbed. Supervise children in the use of the product.

Other Information

SPL UNCLASSIFIED SECTION

  • Avoid extreme temperatures

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Cocamidopropyl PG-Dimonium Chloride Phosphate, Propylene Glycol, Triethylene Glycol, Polysorbate-20

Questions/Comments?

OTC - QUESTIONS SECTION

Call toll free 1-866-323-5465

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel1212

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60867-100-642023-02-06C16284748780-1d6a99b39-46af-a426-e053-dadaa90af4c2safeHands Alcohol Free Hand Sanitizer
60867-100-642022-01-28C16284748780-1d6a99b39-46af-a426-e053-dadaa90af4c2safeHands Alcohol Free Hand Sanitizer

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60867-10060867-100-64

Ingredients#

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

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

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
f3a5e0c5-622a-d7ec-e053-2a95a90a7189848ea30f-5825-40d7-9e74-21299d9c79302023-02-01WarningsExact identifier
spl set id: 848ea30f-5825-40d7-9e74-21299d9c7930

Reported adverse events (FAERS/openFDA)#

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