HOSP CLEAN

Manufacturer
INTERBRILHO HIGIENE E LIMPEZA LTDA | AY CONSULTING SERVICES, LLC
Effective date
2022-01-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:46:49

Label at a glance#

ProductHOSP CLEAN
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) (77%, 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. Aloe Barbadensis Leaf Extract
  3. Carbomer
  4. Denatonium Benzoate
  5. Glycerin
  6. Triethanolamine
  7. 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

Alcohol 77% 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

Aloe Barbadensis Leaf Extract, Carbomer, Denatonium Benzoate, Glycerin, Triethanolamine, water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

4831 mL NDC: 79868-300-01

4831 ml NDC: 79868-300-014831 ml NDC: 79868-300-01

494 mL NDC: 79868-300-02

494 ml NDC: 79868-300-02494 ml NDC: 79868-300-02

483 mL NDC: 79868-300-03

483 ml NDC: 79868-300-03483 ml NDC: 79868-300-03

191 mL NDC: 79868-300-04

191 ml NDC: 79868-300-04191 ml NDC: 79868-300-04

101 mL NDC: 79868-300-05

101 ml NDC: 79868-300-05101 ml NDC: 79868-300-05

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1788839ethanol 77 % Topical GelPSN3
1788839ethanol 0.77 ML/ML Topical GelSCD3
1788839ethanol 77 % Topical GelSY3

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79868-300-01HOSP CLEAN4831 mL in 1 BOTTLE, PLASTICGEL48313
79868-300-02HOSP CLEAN494 mL in 1 BOTTLE, PLASTICGEL4943
79868-300-03HOSP CLEAN483 mL in 1 BOTTLE, PLASTICGEL4833
79868-300-04HOSP CLEAN191 mL in 1 BOTTLE, PLASTICGEL1913
79868-300-05HOSP CLEAN101 mL in 1 BOTTLE, PLASTICGEL1013

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79868-300HOSP CLEAN (ALCOHOL) GEL [INTERBRILHO HIGIENE E LIMPEZA LTDA]3Legacy NDC, 5 package rows20220114_af7652cb-0f64-b2d2-e053-2a95a90a74bc.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
79868-30079868-300-01, 79868-300-02, 79868-300-03, 79868-300-04, 79868-300-05

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
d57b179a-2b95-43b8-e053-2995a90a36ceaf7652cb-0f64-b2d2-e053-2a95a90a74bc2022-01-13WarningsExact identifier
spl id: d57b179a-2b95-43b8-e053-2995a90a36ce
spl set id: af7652cb-0f64-b2d2-e053-2a95a90a74bc

Reported adverse events (FAERS/openFDA)#

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