CC USA Non-Alcohol Foaming Hand Sanitizer

Manufacturer
Coil Chem LLC
Effective date
2020-09-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:29:40

Label at a glance#

ProductCC USA Non-Alcohol Foaming Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure19 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. No rinsing required. Supervise children under 6 years of age when using this product.

Label contents#

Full prescribing information#

Acctive Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use(s)

INDICATIONS & USAGE SECTION

For hand washing to help reduce bacteria that cause disease. For use when soap and water are not available.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

glycerin, decyl glucoside, purified water, aloe vera solution, citric acid.

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product on hands to cover all surfaces. Rub hands together until dry. No rinsing required.

Supervise children under 6 years of age when using this product.

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

Do not get into eyes. If contact offurs, rinse thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation and redness develop.

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.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

999349 mL Tote Label999349 mL Tote LabelNDC: 75508-005-01 999349 mL

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

208198 mL Drum Label208198 mL Drum LabelNDC: 75508-005-02 208198 mL

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3785.41 mL Gallon Label3785.41 mL Gallon LabelNDC: 75508-005-03 3785.41 mL

Package Label - Principla Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1892.7 mL half gallon label1892.7 mL half gallon labelNDC: 75508-005-04 1892.7 mL

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 75508-005-05 946.35 mL 946.35 mL 32 oz Label946.35 mL 32 oz Label

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

473.18 mL 16 oz Label473.18 mL 16 oz LabelNDC: 75508-005-06 473.18 mL

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

236.59 mL 8 oz Label236.59 mL 8 oz LabelNDC: 75508-005-07 236.59 mL

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

177.4 mL 6 oz Label177.4 mL 6 oz LabelNDC: 75508-005-08 177.4 mL

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

118.3 mL 4 oz Label118.3 mL 4 oz LabelNDC: 75508-005-09 118.3 mL

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

59.1 mL 2 oz Label59.1 mL 2 oz LabelNDC: 75508-005-10 59.1 mL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1020365benzalkonium chloride 0.13 % Topical FoamPSN1
1020365benzalkonium chloride 1.3 MG/ML Topical FoamSCD1
1020365benzalkonium chloride 0.13 % Topical FoamSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75508-005-01CC USA Non-Alcohol Foaming Hand Sanitizer999349 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULKLIQUID9993491
75508-005-02CC USA Non-Alcohol Foaming Hand Sanitizer208198 mL in 1 DRUMLIQUID2081981
75508-005-03CC USA Non-Alcohol Foaming Hand Sanitizer3785.41 mL in 1 JUGLIQUID3785.411
75508-005-04CC USA Non-Alcohol Foaming Hand Sanitizer1892.7 mL in 1 JUGLIQUID1892.71
75508-005-05CC USA Non-Alcohol Foaming Hand Sanitizer946.35 mL in 1 BOTTLELIQUID946.351
75508-005-06CC USA Non-Alcohol Foaming Hand Sanitizer473.18 mL in 1 BOTTLELIQUID473.181
75508-005-07CC USA Non-Alcohol Foaming Hand Sanitizer236.59 mL in 1 BOTTLELIQUID236.591
75508-005-08CC USA Non-Alcohol Foaming Hand Sanitizer177.4 mL in 1 BOTTLELIQUID177.41
75508-005-09CC USA Non-Alcohol Foaming Hand Sanitizer118.3 mL in 1 BOTTLELIQUID118.31
75508-005-10CC USA Non-Alcohol Foaming Hand Sanitizer59.1 mL in 1 BOTTLELIQUID59.11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75508-005CC USA NON-ALCOHOL FOAMING HAND SANITIZER (NON-ALCOHOL FOAMING HAND SANITIZER) LIQUID [COIL CHEM LLC]1Legacy NDC, 10 package rows20200918_af837ae3-8e69-740d-e053-2995a90a60e9.zip

Products#

Every source-derived product name is available through these pages.

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NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
af837ae3-8e6a-740d-e053-2995a90a60e9af837ae3-8e69-740d-e053-2995a90a60e92020-09-17WarningsExact identifier
spl id: af837ae3-8e6a-740d-e053-2995a90a60e9
spl set id: af837ae3-8e69-740d-e053-2995a90a60e9

Reported adverse events (FAERS/openFDA)#

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