FDA.reportPublic FDA data

HAND SANITIZER ALOE VERA

Manufacturer
Universal Distribution Center LLC
Effective date
2021-11-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:45:13

Label at a glance#

ProductHAND SANITIZER ALOE VERA
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Hand Sanitizer to help reduce bacteria on skin.

Dosage and administration

• Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry. • Children under 6 years of age should be supervised when using this product.

Storage and handling

• Store below 106 ​ ° F (41°C) • May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

​Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on skin.

WARNINGS

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only.

When using this product, do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach for children. If swallowed, get medical help or contact a Poison Control Center right away.

​Directions:

DOSAGE & ADMINISTRATION SECTION

• Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry.
• Children under 6 years of age should be supervised when using this product.

Other Information:

STORAGE AND HANDLING SECTION

• Store below 106​° F (41°C)
• May discolor certain fabrics or surfaces

​INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Water(Aqua), Aloe Barbadensis Leaf Juice, Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate, Triethanolamine, FD&C Blue No. 1, FD&C Yellow No 5.

SPL UNCLASSIFIED SECTION

With Vitamin E & Other Moisturizers

KILLS GERMS WITHOUT WATER

​UNIVERSAL INSTANT HAND SANITIZER

Made in P.R.C

Distributed by: Universal Distribution Center
96 Distribution Boulevard • Edison, NJ 08817

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52000-115-032023-07-28C16284748780-1e4f33bdf-b304-d8a0-e053-dadaa90a6e4eINSTANT HAND SANITIZER ALOE VERA
52000-115-032022-09-14C16284748780-1e4f33bdf-b304-d8a0-e053-dadaa90a6e4eINSTANT HAND SANITIZER ALOE VERA
52000-115-032022-07-29C16284748780-1e4f33bdf-b304-d8a0-e053-dadaa90a6e4eINSTANT HAND SANITIZER ALOE VERA

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52000-115-03HAND SANITIZER ALOE VERA237 mL in 1 BOTTLE, PUMPGEL2371

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52000-115HAND SANITIZER ALOE VERA (ETHYL ALCOHOL) GEL [UNIVERSAL DISTRIBUTION CENTER LLC]1Legacy NDC, 1 package rows20211201_7d54e7c3-bf39-47a2-98a7-e2e9af18e2f5.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52000-11552000-115-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
TROLAMINE9O3K93S3TKIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
FD&C YELLOW NO. 5I753WB2F1MIACT

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
d757e326-af32-47c9-b499-1ba9d5fd8d2a7d54e7c3-bf39-47a2-98a7-e2e9af18e2f52021-11-24WarningsExact identifier
spl id: d757e326-af32-47c9-b499-1ba9d5fd8d2a
spl set id: 7d54e7c3-bf39-47a2-98a7-e2e9af18e2f5

Reported adverse events (FAERS/openFDA)#

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