FDA.reportPublic FDA data

Dews Plus

Manufacturer
DP IMPORT & EXPORT, INC. | Jinhua Jinshang Tianhua Yizhi Toy Co., Ltd
Effective date
2020-04-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:06:23

Label at a glance#

ProductDews Plus
Active ingredientALCOHOL
Label structure9 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 on hands to cover all surfaces, Rub hands together 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

External use only.

Flammable, Keep away from fire or flame

Do not use

  •  In children less than 2 months of age
  •  On open skin wounds

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 72hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children must be supervised in use of this product.

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

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product on hands to cover all surfaces, Rub hands together until dry

Other Informatin

SPL UNCLASSIFIED SECTION

Store at15°30°c(59"to86F)
Avoid freezing and excessive heat above 40C(104%F)

Inactive Ingredient

INACTIVE INGREDIENT SECTION

water, triethanolamine
glycerin, propylene glycol, Vitamin E, aloe vera gel
carbomer

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN1
1305100ethanol 0.75 ML/ML Topical GelSCD1
1305100ethanol 75 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73824-001-012021-07-23C16284748780-1c7ccaba7-21e1-fd44-e053-dadaa90aa01bDews Plus
73824-001-022021-07-23C16284748780-1c7ccaba7-21e1-fd44-e053-dadaa90aa01bDews Plus
73824-001-032021-07-23C16284748780-1c7ccaba7-21e1-fd44-e053-dadaa90aa01bDews Plus
73824-001-042021-07-23C16284748780-1c7ccaba7-21e1-fd44-e053-dadaa90aa01bDews Plus
73824-001-052021-07-23C16284748780-1c7ccaba7-21e1-fd44-e053-dadaa90aa01bDews Plus
73824-001-062021-07-23C16284748780-1c7ccaba7-21e1-fd44-e053-dadaa90aa01bDews Plus
73824-001-072021-07-23C16284748780-1c7ccaba7-21e1-fd44-e053-dadaa90aa01bDews Plus
73824-001-082021-07-23C16284748780-1c7ccaba7-21e1-fd44-e053-dadaa90aa01bDews Plus
73824-001-092021-07-23C16284748780-1c7ccaba7-21e1-fd44-e053-dadaa90aa01bDews Plus
73824-001-102021-07-23C16284748780-1c7ccaba7-21e1-fd44-e053-dadaa90aa01bDews Plus
73824-001-112021-07-23C16284748780-1c7ccaba7-21e1-fd44-e053-dadaa90aa01bDews Plus
73824-001-122021-07-23C16284748780-1c7ccaba7-21e1-fd44-e053-dadaa90aa01bDews Plus
73824-001-132021-07-23C16284748780-1c7ccaba7-21e1-fd44-e053-dadaa90aa01bDews Plus
73824-001-142021-07-23C16284748780-1c7ccaba7-21e1-fd44-e053-dadaa90aa01bDews Plus
73824-001-152021-07-23C16284748780-1c7ccaba7-21e1-fd44-e053-dadaa90aa01bDews Plus
73824-001-162021-07-23C16284748780-1c7ccaba7-21e1-fd44-e053-dadaa90aa01bDews Plus

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73824-001-01Dews Plus10 mL in 1 POUCHGEL101
73824-001-02Dews Plus15 mL in 1 POUCHGEL151
73824-001-03Dews Plus30 mL in 1 POUCHGEL301
73824-001-04Dews Plus50 mL in 1 POUCHGEL501
73824-001-05Dews Plus60 mL in 1 POUCHGEL601
73824-001-06Dews Plus90 mL in 1 POUCHGEL901
73824-001-07Dews Plus100 mL in 1 POUCHGEL1001
73824-001-08Dews Plus120 mL in 1 BOTTLEGEL1201
73824-001-09Dews Plus125 mL in 1 BOTTLEGEL1251
73824-001-10Dews Plus150 mL in 1 BOTTLEGEL1501
73824-001-11Dews Plus180 mL in 1 BOTTLEGEL1801
73824-001-12Dews Plus237 mL in 1 BOTTLEGEL2371
73824-001-13Dews Plus240 mL in 1 BOTTLEGEL2401
73824-001-14Dews Plus360 mL in 1 BOTTLEGEL3601
73824-001-15Dews Plus480 mL in 1 BOTTLEGEL4801
73824-001-16Dews Plus500 mL in 1 BOTTLEGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73824-001DEWS PLUS (ETHYL ALCOHOL) GEL [DP IMPORT & EXPORT, INC.]1Legacy NDC, 16 package rows20200415_d35128c4-aa6c-4d10-abfe-bf0563effa95.zip

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
73824-00173824-001-01, 73824-001-02, 73824-001-03, 73824-001-04, 73824-001-05, 73824-001-06, 73824-001-07, 73824-001-08, 73824-001-09, 73824-001-10, 73824-001-11, 73824-001-12, 73824-001-13, 73824-001-14, 73824-001-15, 73824-001-16

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
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ISOPROPYL ALCOHOLND2M416302IACT
CAPRYLYL GLYCOL00YIU5438UIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
.ALPHA.-TOCOPHEROL ACETATE, D-A7E6112E4NIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT

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
536d60a4-9f90-454c-b136-df3d0f483db4d35128c4-aa6c-4d10-abfe-bf0563effa952020-04-13WarningsExact identifier
spl id: 536d60a4-9f90-454c-b136-df3d0f483db4
spl set id: d35128c4-aa6c-4d10-abfe-bf0563effa95

Reported adverse events (FAERS/openFDA)#

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