Hand Sanitizer

Manufacturer
AVO TECH INTERNATIONAL INC.
Effective date
2021-12-26
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:45:57

Label at a glance#

ProductHand Sanitizer
Active ingredientISOPROPYL ALCOHOL
Label structure16 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. Carbomer 940
  5. 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, Carbomer 940 purified water USP

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

118 ml Label118 ml Label118 ml NDC: 76600-3070-4

Package label - principal display label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

236 ml Label236 ml Label236 ml NDC: 76600-3070-8

Pakage label - principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

946 ml label946 ml label946 mL NDC: 76600-3070-5

Package label - principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

128 oz Label128 oz Label128 oz NDC: 76600-3070-1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2285607isopropyl alcohol 75 % Topical GelPSN3
2285607isopropyl alcohol 0.75 ML/ML Topical GelSCD3
2285607isopropyl alcohol 75 % Topical GelSY3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76600-3070-12023-01-30C16284748780-1f386c649-dfca-0266-e053-dadaa90a7c1aHand Sanitizer
76600-3070-42023-01-30C16284748780-1f386c649-dfca-0266-e053-dadaa90a7c1aHand Sanitizer
76600-3070-52023-01-30C16284748780-1f386c649-dfca-0266-e053-dadaa90a7c1aHand Sanitizer
76600-3070-82023-01-30C16284748780-1f386c649-dfca-0266-e053-dadaa90a7c1aHand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76600-3070-1Hand Sanitizer3785 mL in 1 BOTTLEGEL37853
76600-3070-4Hand Sanitizer118 mL in 1 BOTTLEGEL1183
76600-3070-5Hand Sanitizer946 mL in 1 BOTTLEGEL9463
76600-3070-8Hand Sanitizer236 mL in 1 BOTTLEGEL2363

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76600-3070HAND SANITIZER (ISOPROPYL ALCOHOL) GEL [AVO TECH INTERNATIONAL INC.]3Legacy NDC, 4 package rows20211227_a49d1ca6-b8b3-434e-e053-2995a90a6e0f.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76600-307076600-3070-4, 76600-3070-8, 76600-3070-5, 76600-3070-1

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 · Source PDF

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
d4149ac0-9c29-014a-e053-2a95a90a1b72a49d1ca6-b8b3-434e-e053-2995a90a6e0f2021-12-26WarningsExact identifier
spl id: d4149ac0-9c29-014a-e053-2a95a90a1b72
spl set id: a49d1ca6-b8b3-434e-e053-2995a90a6e0f

Reported adverse events (FAERS/openFDA)#

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