Hand Sanitizer

Manufacturer
Transliquid Technologies, LLC | Mystic Intl, S.A. DE C.V.
Effective date
2020-06-01
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:15:36

Label at a glance#

ProductHand Sanitizer 8oz
Active ingredientALCOHOL
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. Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (80%, volume/volume (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

Ethyl Alcohol 70% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitzer

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.

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 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, triethanolamine, carbomer 940, purified water USP

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

120 mL NDC: 75477-435-12

FRONT 120MLFRONT 120ML

BACK 120MLBACK 120ML

250 mL NDC: 75477-435-25

250ML FRONT250ML FRONT

250MLBACK250MLBACK

500 mL NDC: 75477-435-50

500MLFRONT500MLFRONT

500MLBACK500MLBACK


02 mL NDC: 75477-435-02

SFRONTSFRONT

SBACKSBACK


1000 L NDC: 75477-435-10
TOTETOTE

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75477-435-02Hand Sanitizer8oz2 mL in 1 POUCHGEL24
75477-435-10Hand Sanitizer8oz1000000 mL in 1 BOTTLEGEL10000004
75477-435-12Hand Sanitizer8oz120 mL in 1 BOTTLE, PLASTICGEL1204
75477-435-25Hand Sanitizer8oz250 mL in 1 BOTTLE, PLASTICGEL2504
75477-435-50Hand Sanitizer8oz500 mL in 1 BOTTLE, PLASTICGEL5004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75477-435HAND SANITIZER 8OZ (ALCOHOL) GEL [TRANSLIQUID TECHNOLOGIES, LLC]4Legacy NDC, 5 package rows20200602_a3d0e7ee-84d9-bbb8-e053-2995a90a053b.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
75477-43575477-435-25, 75477-435-50, 75477-435-02, 75477-435-10, 75477-435-12

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
a70b76cf-eaf3-cfe0-e053-2a95a90a66fba3d0e7ee-84d9-bbb8-e053-2995a90a053b2020-06-01WarningsExact identifier
spl id: a70b76cf-eaf3-cfe0-e053-2a95a90a66fb
spl set id: a3d0e7ee-84d9-bbb8-e053-2995a90a053b

Reported adverse events (FAERS/openFDA)#

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