Hand Sanitizer with Moisturizers and Aloe Vera

Manufacturer
Family Dollar Services Inc. | Delta Kozmetik Sanayi Ve Ticaret-Selim Yesil
Effective date
2021-01-15
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 23:36:58

Label at a glance#

ProductHand Sanitizer with Moisturizers and Aloe Vera Modesa
Active ingredientALCOHOL
Label structure11 sections

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

hand sanitizer to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

Flammable. Keep away from fire and flame. For external use only

When using this product

OTC - WHEN USING SECTION

■ do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and aska doctor if

OTC - STOP USE SECTION

■ irritation or rash appears and lasts

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 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

SPL UNCLASSIFIED SECTION

■ store below 106ºF (41ºC) ■ may discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, propylene glycol, acrylates/c10-30 alkyl acrylate crosspolymer, isopropyl alcohol,aminomethylpropanol, isopropyl myristate, caprylyl glycol, phenoxyethanol, fragrance, tocopheryl acetate, aloe barbedensis leaf juice, FD&C yellow no. 5, FD&C blue no. 1

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55319-43255319-432-08, 55319-432-33, 55319-432-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
b8f48f44-f66f-d652-e053-2995a90a1ad86142ca63-dfc1-0541-e053-2a91aa0a6adb2021-01-15WarningsExact identifier
spl id: b8f48f44-f66f-d652-e053-2995a90a1ad8
spl set id: 6142ca63-dfc1-0541-e053-2a91aa0a6adb

Reported adverse events (FAERS/openFDA)#

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