CLEACE

Manufacturer
Nanjing Aogrand Int'l Corp
Effective date
2020-04-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:05:46

Label at a glance#

ProductCLEACE
Active ingredientALCOHOL
Label structure19 sections

Indications and uses

hand sanitizer to help decrease bacteria on the skin, when water, soap & towel are not available. recommended for repeated use.

Dosage and administration

place enough product into your palms and thoroughly spread on both hands. rub into skin until dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • hand sanitizer to help decrease bacteria on the skin, when water, soap & towel are not available.
  • recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire or flame.

Do not apply around eyes. Do not use in ears & mouth.

When using this product, avoid contact with eyes. In case of contact flush eyes with water.

Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children must be supervised in use of this product.

Directions

DOSAGE & ADMINISTRATION SECTION

  • place enough product into your palms and thoroughly spread on both hands.
  • rub into skin until dry.

Other information

SPL UNCLASSIFIED SECTION

  • store below 110°F (43°C).
  • may discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

carbomer, triethanolamine, glycerin, water

1oz CLEACE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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2oz CLEACE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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3.4oz CLEACE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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8oz CLEACE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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10oz CLEACE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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16.9oz CLEACE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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33.8oz CLEACE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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39.9oz CLEACE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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50.7 oz CLEACE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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169.1oz CLEACE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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676.3oz CLEACE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74621-002-01CLEACE30 mL in 1 BOTTLE, PLASTICGEL301
74621-002-02CLEACE60 mL in 1 PACKAGEGEL601
74621-002-03CLEACE100 mL in 1 BOTTLE, PLASTICGEL1001
74621-002-04CLEACE237 mL in 1 BOTTLE, PLASTICGEL2371
74621-002-05CLEACE296 mL in 1 BOTTLE, PLASTICGEL2961
74621-002-06CLEACE500 mL in 1 BOTTLE, PLASTICGEL5001
74621-002-07CLEACE1000 mL in 1 BOTTLE, PLASTICGEL10001
74621-002-08CLEACE1180 mL in 1 BOTTLE, PLASTICGEL11801
74621-002-09CLEACE1500 mL in 1 BOTTLE, PLASTICGEL15001
74621-002-10CLEACE5000 mL in 1 BOTTLE, PLASTICGEL50001
74621-002-11CLEACE20000 mL in 1 BOTTLE, PLASTICGEL200001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74621-002CLEACE (ETHYL ALCOHOL) GEL [NANJING AOGRAND INT'L CORP]1Legacy NDC, 11 package rows20200410_d9b2b5a2-380b-41d8-927b-c15fcc4a94a2.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
9f432ee2-549f-4c86-9aa5-4ced447f4bf0d9b2b5a2-380b-41d8-927b-c15fcc4a94a22020-04-07WarningsExact identifier
spl id: 9f432ee2-549f-4c86-9aa5-4ced447f4bf0
spl set id: d9b2b5a2-380b-41d8-927b-c15fcc4a94a2

Reported adverse events (FAERS/openFDA)#

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