CC USA Best 70% Gel Hand Sanitizer

Manufacturer
Coil Chem LLC
Effective date
2020-05-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:19:48

Label at a glance#

ProductCC USA Best 70% Gel Hand Sanitizer
Active ingredientALCOHOL
Label structure21 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 70.5% 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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Tote Label 999349 mLTote Label 999349 mL999349 mL NDC: 75508-003-01

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Gallon Label 3785.41 mLGallon Label 3785.41 mL3785.41 mL NDC: 75508-003-02

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Half Gallon Label 1892.71 mLHalf Gallon Label 1892.71 mL1892.71 mL NDC: 75508-003-03

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

32oz Label 946.35 mL32oz Label 946.35 mL946.35 mL NDC: 75508-003-04

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

16oz Label 473.176 mL16oz Label 473.176 mL473.176 mL NDC: 75508-003-04

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

8oz Label 236.588 mL8oz Label 236.588 mL236.588 mL NDC: 75508-003-06

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

177.4 mL 6 oz Label177.4 mL 6 oz Label177.4 mL NDC: 75508-003-07

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

118.3 mL 4oz Label118.3 mL 4oz Label118.3 mL NDC: 75508-003-08

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

59 mL 2oz Label59 mL 2oz Label59.147 mL NDC: 75508-003-09

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
75508-003-01CC USA Best 70% Gel Hand Sanitizer999349 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULKGEL9993492
75508-003-02CC USA Best 70% Gel Hand Sanitizer3785.41 mL in 1 JUGGEL3785.412
75508-003-03CC USA Best 70% Gel Hand Sanitizer1892.71 mL in 1 JUGGEL1892.712
75508-003-04CC USA Best 70% Gel Hand Sanitizer946.35 mL in 1 BOTTLEGEL946.352
75508-003-05CC USA Best 70% Gel Hand Sanitizer473.176 mL in 1 BOTTLEGEL473.1762
75508-003-06CC USA Best 70% Gel Hand Sanitizer236.588 mL in 1 BOTTLEGEL236.5882
75508-003-07CC USA Best 70% Gel Hand Sanitizer177.441 mL in 1 BOTTLEGEL177.4412
75508-003-08CC USA Best 70% Gel Hand Sanitizer118.294 mL in 1 BOTTLEGEL118.2942
75508-003-09CC USA Best 70% Gel Hand Sanitizer59.147 mL in 1 BOTTLEGEL59.1472

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75508-003CC USA BEST 70% GEL HAND SANITIZER (ALCOHOL) GEL [COIL CHEM LLC]2Legacy NDC, 9 package rows20200702_a4d9e594-a820-2236-e053-2995a90ae83c.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
a62f5593-b8de-4410-e053-2995a90a6c29a4d9e594-a820-2236-e053-2995a90ae83c2020-05-21WarningsExact identifier
spl id: a62f5593-b8de-4410-e053-2995a90a6c29
spl set id: a4d9e594-a820-2236-e053-2995a90ae83c

Reported adverse events (FAERS/openFDA)#

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