FDA.reportPublic FDA data

DayClear Hand Sanitizer Gel

Manufacturer
GM Pharmaceuticals, Inc
Effective date
2020-04-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:34:45

Label at a glance#

ProductDayClear Hand Sanitizer Gel
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

■ put enough product in your palm to cover all surfaces of both hands and rub hands together briskly until dry ■ children under 6 years should be supervised when using this product

Storage and handling

Store between 20-30ºC (68-86ºF)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62% v/v

Purpose(s)

OTC - PURPOSE SECTION

Antimicrobial

Use(s)

INDICATIONS & USAGE SECTION

■ hand sanitizer to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire or flame.

When using this product

OTC - WHEN USING SECTION

do not use in or near the eyes.

In case of contact, rinse eyes thoroghyly with water.

Stop Use and Ask a Doctor if

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts

Keep Out Of Reach Of Children

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

■ put enough product in your palm to cover all surfaces of both hands and rub hands together briskly until dry

■ children under 6 years should be supervised when using this product

Other Information

STORAGE AND HANDLING SECTION

Store between 20-30ºC (68-86ºF)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Carbomer, Chamomilla rectita (matricaria) flower extract, Diisopropylamine, Glycerin, Isopropyl myristate, Water

Questions?

OTC - QUESTIONS SECTION

Call 1-888-535-0305

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DayClear Hand Sanitizer Gel

NDC 58809-226-02


2 fl.oz (59mL)

PDpPDp

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58809-226-022022-03-09C16284748780-1d6a99b39-3ace-a426-e053-dadaa90af4c2DayClear Hand Sanitizer Gel 2oz Tube
58809-226-022022-01-28C16284748780-1d6a99b39-3ace-a426-e053-dadaa90af4c2DayClear Hand Sanitizer Gel 2oz Tube

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58809-22658809-226-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CARBOMER 9804Q93RCW27EIACT
GLYCERINPDC6A3C0OXIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
MATRICARIA CHAMOMILLAG0R4UBI2ZZIACT
ALOE VERA LEAFZY81Z83H0XIACT
DIISOPROPYLAMINEBR9JLI40NOIACT
ALCOHOL3K9958V90MACTIB

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
d9d44785-4265-ef7e-e053-2995a90a7ddba3bb5c0d-52da-75d6-e053-2995a90abbc72022-03-09WarningsExact identifier
spl set id: a3bb5c0d-52da-75d6-e053-2995a90abbc7

Reported adverse events (FAERS/openFDA)#

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