FDA.reportPublic FDA data

HAND SANITIZER ANTIBACTERIAL WITH MOISTURIZERS AND ALOE 8OZ

Manufacturer
Ningbo Liyuan Daily Chemical Products Co.,Ltd.
Effective date
2022-10-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:51:04

Label at a glance#

ProductHAND SANITIZER ANTIBACTERIAL WITH MOISTURIZERS AND ALOE 8OZ
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

hand sanitizer to help reduce bacteria on the skin.

Dosage and administration

wet hands thoroughly with product and rub into skin until dry. Children under 6 years of age should be supervised by an adult when using this product.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62.0%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

hand sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

WARNINGS SECTION

Flammable. Keep away from heat and flame.

When using this product

OTC - WHEN USING SECTION

avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or redness develops.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center.

Directions

DOSAGE & ADMINISTRATION SECTION

  • wet hands thoroughly with product and rub into skin until dry.
  • Children under 6 years of age should be supervised by an adult when using this product.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water (aqua), aloe barbadensis (aloe vera) leaf juice, carbomer, fragrance, glycerin, propylene glycol, tocopheryl acetate (vitamin E), triethanolamine, FD&C blue no. 1, FD&C yellow no.5

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76176-06176176-061-01

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
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
CARBOMER 934Z135WT9208IACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CUPRIC BIS(TRIETHANOLAMINE)YBM44X0B6HIACT
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
FD&C YELLOW NO. 5I753WB2F1MIACT
FD&C BLUE NO. 1H3R47K3TBDIACT

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
ebc34633-f2b6-b47e-e053-2a95a90a372c8c0e6bc3-f97b-b671-e053-2a95a90ab6a82022-10-24WarningsExact identifier
spl id: ebc34633-f2b6-b47e-e053-2a95a90a372c
spl set id: 8c0e6bc3-f97b-b671-e053-2a95a90ab6a8

Reported adverse events (FAERS/openFDA)#

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