Hand Sanitizer

Manufacturer
Sustainable Tech LLC
Effective date
2020-05-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:15:46

Label at a glance#

ProductHand Sanitizer
Active ingredientISOPROPYL ALCOHOL
Label structure13 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

This is a hand sanitizer manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency (CoViD-19); Guidance for Industry.

The hand sanitizer is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:

  1. Isopropyl Alcohol (75%, v/v) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
  2. Glycerol (1.45% v/v).
  3. Hydrogen peroxide (0.125% v/v).
  4. Sterile distilled water or boiled cold water.

The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

glycerin, hydrogen peroxide, purified water USP

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60 ml NDC: 77282-333-02 60ml label60ml label118ml NDC: 77282-333-04 118ml Lable118ml Lable236ml NDC:77282-333-08 236ml Lable236ml Lable473ml NDC:77282-333-16 473ml lable473ml lable591ml NDC:77282-333-20 591ml lable591ml lable946ml NDC:77282-333-32 946ml Lable946ml Lable3785ml NDC:77282-333-11 3785ml Lable3785ml Lable18927ml NDC:77282-333-05 18927ml Label18927ml Label208197ml NDC:77282-333-55 208197ml Label208197ml Label

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77282-333-02Hand Sanitizer60 mL in 1 BOTTLEGEL601
77282-333-04Hand Sanitizer118 mL in 1 BOTTLEGEL1181
77282-333-08Hand Sanitizer236 mL in 1 BOTTLEGEL2361
77282-333-11Hand Sanitizer3785 mL in 1 BOTTLEGEL37851
77282-333-15Hand Sanitizer18927 mL in 1 BOTTLEGEL189271
77282-333-16Hand Sanitizer473 mL in 1 BOTTLEGEL4731
77282-333-20Hand Sanitizer591 mL in 1 BOTTLEGEL5911
77282-333-32Hand Sanitizer946 mL in 1 BOTTLEGEL9461
77282-333-55Hand Sanitizer208197 mL in 1 BOTTLEGEL2081971

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77282-333HAND SANITIZER (ISOPROPYL ALCOHOL) GEL [SUSTAINABLE TECH LLC]1Legacy NDC, 9 package rows20200603_a6accce4-3dc1-e8eb-e053-2a95a90a4190.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
a6acd1d9-4f9f-692a-e053-2a95a90a5697a6accce4-3dc1-e8eb-e053-2a95a90a41902020-05-27WarningsExact identifier
spl id: a6acd1d9-4f9f-692a-e053-2a95a90a5697
spl set id: a6accce4-3dc1-e8eb-e053-2a95a90a4190

Reported adverse events (FAERS/openFDA)#

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