Hand Sanitizer

Manufacturer
Sun Coast Resources, Inc. | Genesis Custom Chemical Blending
Effective date
2020-08-04
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:23:52

Label at a glance#

ProductHand Sanitizer
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

Alcohol 80% 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, purified water USP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

118.3 mL NDC: 75343-004-10

4 oz King Fuels4 oz King Fuels208200 mL NDC: 75343-004-09 55 Gal label55 Gal label

18900 mL NDC: 75343-004-08 5 Gal label5 Gal label

950 mL NDC: 75343-004-07 1 Qt label1 Qt label

499.87 mL NDC: 75343-004-06 16.9 oz label16.9 oz label

354.9 mL NDC: 75343-004-05 12 oz label12 oz label

236.6 mL NDC: 75343-004-04 8 oz label8 oz label

177.4 mL NDC: 75343-004-03 6 oz label6 oz label

118.3 mL NDC: 75343-004-02 4 oz label4 oz label

88.8 mL NDC: 75343-004-01

3 oz label3 oz label

DailyMed Product Concepts#

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

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75343-004-01Hand Sanitizer88.8 mL in 1 BOTTLE, PLASTICLIQUID88.83
75343-004-02Hand Sanitizer118.3 mL in 1 BOTTLE, PLASTICLIQUID118.33
75343-004-03Hand Sanitizer177.4 mL in 1 BOTTLE, PLASTICLIQUID177.43
75343-004-04Hand Sanitizer236.6 mL in 1 BOTTLE, PLASTICLIQUID236.63
75343-004-05Hand Sanitizer354.9 mL in 1 BOTTLE, PLASTICLIQUID354.93
75343-004-06Hand Sanitizer499.8 mL in 1 BOTTLE, PLASTICLIQUID499.83
75343-004-07Hand Sanitizer950 mL in 1 BOTTLE, PLASTICLIQUID9503
75343-004-08Hand Sanitizer18900 mL in 1 PAILLIQUID189003
75343-004-09Hand Sanitizer208200 mL in 1 DRUMLIQUID2082003
75343-004-10Hand Sanitizer118.3 mL in 1 BOTTLE, PLASTICLIQUID118.33

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75343-004HAND SANITIZER (ALCOHOL) LIQUID [SUN COAST RESOURCES, INC.]3Legacy NDC, 10 package rows20200806_a4494957-4334-97e0-e053-2995a90a0e19.zip

Products#

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NDC Codes#

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ac1080c1-00fa-e05a-e053-2a95a90a17f4a4494957-4334-97e0-e053-2995a90a0e192020-08-04WarningsExact identifier
spl id: ac1080c1-00fa-e05a-e053-2a95a90a17f4
spl set id: a4494957-4334-97e0-e053-2995a90a0e19

Reported adverse events (FAERS/openFDA)#

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