Kelley's Advanced Hand Sanitizer Gel

Manufacturer
K2 Distribution Company LP
Effective date
2020-10-01
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:06:56

Label at a glance#

ProductKelleys Advanced Hand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

to help reduce bacteria on the skin that can cause disease recommended for repeated use

Dosage and administration

apply liberally to hands to cover all surfaces rub hands together until dry supervise children under 6 years old not recommended for infants

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 65%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • to help reduce bacteria on the skin that can cause disease
  • recommended for repeated use

Warnings

WARNINGS SECTION

For external use only

Flammable, keep away from fire or flame.

OTC - WHEN USING SECTION

When using this product avoid contact with the eyes. In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness appears and lasts more than 72 hours

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply liberally to hands to cover all surfaces
  • rub hands together until dry
  • supervise children under 6 years old
  • not recommended for infants

Other information

SPL UNCLASSIFIED SECTION

Store between 0°C (32°F) - 41°C (105°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, acrylates copolymer, glycerin, aloe barbadensis (aloe) extract, fragrance, sodium hydroxide

OTC - QUESTIONS SECTION

Questions? 888-458-1038

SPL UNCLASSIFIED SECTION

Kelley's Adanced Hand Sanitizer Gel

WITH MOISTURIZING ALOE

1 Gallon (3.78L)

Triclosan, sulfate & paraben-free

NOT FOR RESALE

Distributed by:

K2 Distribution Company LP

950 Loveridge Rd, Pittsburgh, CA 94565

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78039-06278039-062-01, 78039-062-02

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
d66a2ce7-46ed-2e63-e053-2a95a90abd46abc4959e-0d4d-26bc-e053-2995a90af2d92022-01-25WarningsExact identifier
spl set id: abc4959e-0d4d-26bc-e053-2995a90af2d9

Reported adverse events (FAERS/openFDA)#

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