CLAYR

Manufacturer
Sunbio Corporation
Effective date
2021-01-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:54:31

Label at a glance#

ProductCLAYR
Active ingredientALCOHOL, CINNAMON OIL, CITRIC ACID MONOHYDRATE
Label structure12 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Product NDC: 81311-025:

Directions: 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.

INACTIVE INGREDIENT SECTION

Product NDC: 81311-025:

HYDROGEN PEROXIDE, GLYCERIN, CINNAMON OIL, ANHYDROUS CITRIC ACID, WATER

INDICATIONS & USAGE SECTION

Product NDC: 81311-025:

Use(s): Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Product NDC: 81311-025:

If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

OTC - PURPOSE SECTION

Product NDC: 81311-025:

Antiseptic

OTC - ACTIVE INGREDIENT SECTION

Product NDC: 81311-025:

Alcohol 80% v/v

WARNINGS SECTION

Product NDC: 81311-025:

For external use only. Flammable. Keep away from heat or flame

OTC - DO NOT USE SECTION

Product NDC: 81311-025:

in children less than 2 months of age • on open skin wounds

OTC - WHEN USING SECTION

Product NDC: 81311-025:

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Product NDC: 81311-025:

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

OTHER SAFETY INFORMATION

Product NDC: 81311-025:

Store between 15-30C (59-86F)

• Avoid freezing and excessive heat above 40C (104F)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60 mL NDC: 81311-015-60 60 mL NDC: 81311-015-60 label60 mL NDC: 81311-015-60 label

300 mL NDC: 81311-015-30 300 mL NDC: 81311-015-30 label300 mL NDC: 81311-015-30 label

1000 mL NDC: 81311-015-10 1000 mL NDC: 81311-015-10 label1000 mL NDC: 81311-015-10 label

3785 mL NDC: 81311-015-37 3785 mL NDC: 81311-015-37 label3785 mL NDC: 81311-015-37 label

60 mL NDC: 81311-025-60 60 mL NDC: 81311-025-60 label60 mL NDC: 81311-025-60 label

300 mL NDC: 81311-025-30 300 mL NDC: 81311-025-30 label300 mL NDC: 81311-025-30 label

1000 mL NDC: 81311-025-10 1000 mL NDC: 81311-025-10 label1000 mL NDC: 81311-025-10 label

3785 mL NDC: 81311-025-37 3785 mL NDC: 81311-025-37 label3785 mL NDC: 81311-025-37 label

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
d30a0f73-4c6c-9f05-e053-2995a90a50e4b6d727f2-29ff-3d0a-e053-2995a90a92172021-12-13WarningsExact identifier
spl set id: b6d727f2-29ff-3d0a-e053-2995a90a9217

Reported adverse events (FAERS/openFDA)#

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