Hand Sanitizer Foam

Manufacturer
Custom Chemical Solutions | Kutol Products Company
Effective date
2024-01-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:07:42

Label at a glance#

ProductHand Sanitizer Foam
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

To decrease bacteria on the skin that could cause disease Recommended for repeated use

Dosage and administration

Pump enough product into palm of hand to thoroughly cover all surfaces of both hands. Rub hands together briskly until dry. For children under 6, use only under adult supervision.

Storage and handling

Store below 110 F (43 C). May discolor some fabrics. May be harmful to wood finishes and plastics.

Label contents#

Full prescribing information#

Active ingredients (v/v)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • To decrease bacteria on the skin that could cause disease
  • Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only: hands

Flammable. Keep away from fire or flame.

OTC - WHEN USING SECTION

When using this productavoid contact with eyes.

In case of eye contact, flush eyes with water.

Avoid contact with broken skin.

Do not ingest or inhale.

OTC - STOP USE SECTION

Stop use and ask a doctorif irritation or redness develops, or if condition persists for 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 right away.

Directions:

DOSAGE & ADMINISTRATION SECTION

Pump enough product into palm of hand to thoroughly cover all surfaces of both hands.

Rub hands together briskly until dry.

For children under 6, use only under adult supervision.

Other information:

STORAGE AND HANDLING SECTION

Store below 110 F (43 C).

May discolor some fabrics.

May be harmful to wood finishes and plastics.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Water (Eau), Bis-PEG-10 Dimethicone, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Denatonium Benzoate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

container labelHSF1container labelHSF1

HAND

SANITIZER

FOAM

UniFirst Corporation 88UF 1L (1000 mL, 33.8 US fl. oz.)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
616805ethanol 70 % Topical FoamPSN2
616805ethanol 0.7 ML/ML Topical FoamSCD2
616805ethanol 70 % Topical FoamSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77955-002-02Hand Sanitizer Foam1000 mL in 1 BOTTLESOLUTION10002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77955-002HAND SANITIZER FOAM (ALCOHOL) SOLUTION [CUSTOM CHEMICAL SOLUTIONS]2Current NDC, Legacy NDC, 1 package rows20240123_b0f1cb6f-0b47-7652-e053-2a95a90a7c6b.zip

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
77955-00277955-002-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
Hand Sanitizer FoamALCOHOLCustom Chemical Solutionsb0f1cb6f-0b47-7652-e053-2a95a90a7c6b2024-01-22WarningsExact identifier
ndc (package): 77955-002-02
ndc (product): 77955-002
ndc11 (package): 77955000202
spl id: 0f8c7c79-62a8-3513-e063-6294a90a16df
spl set id: b0f1cb6f-0b47-7652-e053-2a95a90a7c6b

Reported adverse events (FAERS/openFDA)#

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