Bocchi Laboratories Liquid Hand Sanitizer

Manufacturer
Bocchi Laboratories
Effective date
2020-05-08
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:32:03

Label at a glance#

ProductBocchi Laboratories Liquid Hand Sanitizer
Active ingredientALCOHOL
Label structure13 sections

Storage and handling

Other information Store between 15°-30°C (59°-86°F). Avoid freezing and excessive heat about 40°C (104°F)

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Alcohol 80% v/v

OTC - PURPOSE SECTION

Purpose

Antiseptic

WARNINGS SECTION

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

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears and mouth. In case of contact with eyes, rinse 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 a Poison Control Center right away.

INDICATIONS & USAGE SECTION

Uses

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

DOSAGE & ADMINISTRATION SECTION

Directions

  • 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 SECTION

Other information

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

INACTIVE INGREDIENT SECTION

Inactive ingredients Glycerin, Hydrogen Peroxide, Purified Water USP

OTC - DO NOT USE SECTION

Do not use

  • In children less than 2 months of age
  • On open skin wounds

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:

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.
Glycerol (1.45% v/v).
Hydrogen peroxide (0.125% v/v).
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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BLLHS1BLLHS1BLLHS2BLLHS2

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57702-10157702-101-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
a51c4bf1-8a52-357d-e053-2995a90a81eea36fecc1-00c2-aa23-e053-2995a90ad2f52020-05-08WarningsExact identifier
spl id: a51c4bf1-8a52-357d-e053-2995a90a81ee
spl set id: a36fecc1-00c2-aa23-e053-2995a90ad2f5

Reported adverse events (FAERS/openFDA)#

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