UCARE HAND SANITIZER

Manufacturer
Open Door Packaging, Llc
Effective date
2020-05-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:15:23

Label at a glance#

ProductUCARE HAND SANITIZER
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

• 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.

Storage and handling

• Store between 15-30C (59-86F) • Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Active ingredient[s]

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

Warnings For external use only. Flammable.

Keep away from heat or flame

Do not use

• on children less than 2 months of age

• on open skin wounds

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

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

• 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.

Other Information

STORAGE AND HANDLING SECTION

• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

INACTIVE INGREDIENT SECTION

Inactive ingredients deionized water, carbomer,  glycerin,  triethanolamine

SPL UNCLASSIFIED SECTION

ucare FOUNDATION

Non-Sterile Solution

Moisturize your hands while decreasing bacteria.

usmooth

UNEXPECTED LUXURY

Springfield, MO 65803

Made in USA

usmooth.com

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackagingPackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN2
582753ethanol 0.7 ML/ML Topical SolutionSCD2
582753ethanol 70 % Topical SolutionSY2
582753ethyl alcohol 70 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78086-905-02UCARE HAND SANITIZER60 mL in 1 BOTTLE, PLASTICSOLUTION602
78086-905-04UCARE HAND SANITIZER118.3 mL in 1 BOTTLE, PLASTICSOLUTION118.32
78086-905-08UCARE HAND SANITIZER236 mL in 1 BOTTLE, PLASTICSOLUTION2362
78086-905-12UCARE HAND SANITIZER354 mL in 1 BOTTLE, PLASTICSOLUTION3542
78086-905-16UCARE HAND SANITIZER473 mL in 1 BOTTLE, PLASTICSOLUTION4732
78086-905-28UCARE HAND SANITIZER3785 mL in 1 BOTTLE, PLASTICSOLUTION37852
78086-905-64UCARE HAND SANITIZER1892 mL in 1 BOTTLE, PLASTICSOLUTION18922
78086-905-85UCARE HAND SANITIZER250 mL in 1 BOTTLE, PLASTICSOLUTION2502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78086-905UCARE HAND SANITIZER (ETHYL ALCOHOL) SOLUTION [OPEN DOOR PACKAGING, LLC]2Legacy NDC, 8 package rows20200531_49df0c4d-5778-4018-a418-e1bef0c7b883.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
f676cb73-1a21-4e7d-bb10-e6515e789f2049df0c4d-5778-4018-a418-e1bef0c7b8832020-05-28WarningsExact identifier
spl id: f676cb73-1a21-4e7d-bb10-e6515e789f20
spl set id: 49df0c4d-5778-4018-a418-e1bef0c7b883

Reported adverse events (FAERS/openFDA)#

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