DR.DAVEY

Manufacturer
SHANTOU S.E.Z BAOJIE INDUSTRY CO., LTD
Effective date
2020-04-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:07:46

Label at a glance#

ProductDR.DAVEY
Active ingredientALCOHOL
Label structure10 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 lngredient  

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.

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.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children must be supervised in use of this product.

Other information

SPL UNCLASSIFIED SECTION

• store below 110℉ (43℃).
• may discolor certain fabrics or surfaces.

Inactive ingredient

INACTIVE INGREDIENT SECTION

carbomer, triethanolamine, glycerin, water.

Product labels

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1047755ethanol 75 % Topical SolutionPSN1
1047755ethanol 0.75 ML/ML Topical SolutionSCD1
1047755ethanol 75 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74913-001-012022-01-28C16284748780-1d6a99b39-d76a-a426-e053-dadaa90af4c2420918bd-5c52-41ea-acd9-3dd703f22509
74913-001-022022-01-28C16284748780-1d6a99b39-d76a-a426-e053-dadaa90af4c2420918bd-5c52-41ea-acd9-3dd703f22509

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74913-001-01DR.DAVEY100 mL in 1 BOTTLE, PLASTICLIQUID1001
74913-001-02DR.DAVEY500 mL in 1 BOTTLE, PLASTICLIQUID5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74913-001DR.DAVEY (ETHYL ALCOHOL) LIQUID [SHANTOU S.E.Z BAOJIE INDUSTRY CO., LTD]1Legacy NDC, 2 package rows20200425_420918bd-5c52-41ea-acd9-3dd703f22509.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74913-00174913-001-01, 74913-001-02

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 · Source PDF

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
9f00be86-c51b-44f7-9367-f541b7eeaa3f420918bd-5c52-41ea-acd9-3dd703f225092020-04-24WarningsExact identifier
spl id: 9f00be86-c51b-44f7-9367-f541b7eeaa3f
spl set id: 420918bd-5c52-41ea-acd9-3dd703f22509

Reported adverse events (FAERS/openFDA)#

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