Dosoon Alcohol Hand Sanitizer

Manufacturer
YINGDE DOSOON FINE CHEMICAL CO.,LTD
Effective date
2021-01-11
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:57:17

Label at a glance#

ProductDosoon Alcohol Hand Sanitizer
Active ingredientALCOHOL
Label structure8 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#

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 & Purpose

OTC - ACTIVE INGREDIENT SECTION

Antiseptic, Hand Sanitizer

OTC - PURPOSE SECTION

Active ingredientPurpose
Alcohol 80% v/v ..............Antiseptic

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

When using this product

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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: 75608-001-01 60 ml round bottle label60 ml round bottle label

60 mL NDC: 75608-001-02 60 ml flat bottle label60 ml flat bottle label

80 mL NDC: 75608-001-03 80 ml tube label80 ml tube label

100 mL NDC: 75608-001-04 100 ml bottle label100 ml bottle label

100 mL NDC: 75608-001-05 100 ml tube label100 ml tube label

180 mL NDC: 75608-001-06 180 ml bottle label180 ml bottle label

290 mL NDC: 75608-001-07 290 ml bottle label290 ml bottle label

480 mL NDC: 75608-001-08 480 ml bottle label480 ml bottle label

Products#

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NDC Codes#

Ingredients#

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

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Source Document#

Source XML · Source PDF

openFDA label cross-check#

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
e5eb3865-334e-5345-e053-2995a90ae15ca2d57b8b-6d83-58cc-e053-2995a90afafe2022-08-10WarningsExact identifier
spl set id: a2d57b8b-6d83-58cc-e053-2995a90afafe

Reported adverse events (FAERS/openFDA)#

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