Handy Solutions Hand Sanitizer

Manufacturer
Navajo Manufacturing Company Inc. | Nantong Health & Beyond Hygienic Products Inc.
Effective date
2024-04-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:11:04

Label at a glance#

ProductHandy Solutions Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

A hand sanitizer to help reduce bacteria on the skin

Dosage and administration

Put enough product in your palm to cover hands and rub hands together briskly until dry. Children under 6 years of age should be supervised when using this product.

Storage and handling

Store below 110°F (43°C). May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • A hand sanitizer to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only.

OTC - WHEN USING SECTION

When using this product do not use in or near eyes. In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts.

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

  • Put enough product in your palm to cover hands and rub hands together briskly until dry.
  • Children under 6 years of age should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

  • Store below 110°F (43°C).
  • May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Juice, Fragrance(Parfum), Glycerin, Maltodextrin, Propylene Glycol, Tocopheryl Acetate, Triethanolamine, Water(Aqua).

Questions or comments?

OTC - QUESTIONS SECTION

Call 1-800-525-5097

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Handy Solutions Hand SanitizerHandy Solutions Hand Sanitizer

Carded Handy Solutions Hand SanitizerCarded Handy Solutions Hand Sanitizer

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN1
582753ethanol 0.7 ML/ML Topical SolutionSCD1
582753ethanol 70 % Topical SolutionSY1
582753ethyl alcohol 70 % Topical SolutionSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67751-086-01Handy Solutions Hand Sanitizer59 mL in 1 BOTTLELIQUID591
67751-086-02Handy Solutions Hand Sanitizer59 mL in 1 BOTTLELIQUID591
67751-086-02Handy Solutions Hand Sanitizer1 in 1 PACKAGELIQUID11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67751-086HANDY SOLUTIONS HAND SANITIZER (ALCOHOL) LIQUID [NAVAJO MANUFACTURING COMPANY INC.]1Current NDC, 3 package rows20240417_16252cb5-2db7-cf69-e063-6394a90aefb1.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
67751-08667751-086-02, 67751-086-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
Handy Solutions Hand SanitizerALCOHOLNavajo Manufacturing Company Inc.16252cb5-2db7-cf69-e063-6394a90aefb12024-04-15WarningsExact identifier
ndc (package): 67751-086-02
ndc (package): 67751-086-01
ndc (product): 67751-086
ndc11 (package): 67751008601
ndc11 (package): 67751008602
spl id: 16252cbf-a378-1bbe-e063-6294a90a0ee6
spl set id: 16252cb5-2db7-cf69-e063-6394a90aefb1

Reported adverse events (FAERS/openFDA)#

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