LUCKY Hand Sanitizer INSTANT Vitamin E

Manufacturer
Delta Brands Inc
Effective date
2023-06-22
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:29:44

Label at a glance#

ProductLUCKY Hand Sanitizer INSTANT Vitamin E PREFERRED FORMULA
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

■ place enough product in your palm ■ rub hands vigorously 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 62% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

hand sanitizer to help reduce bacteria on the skin that could cause disease

Warnings

WARNINGS SECTION

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

When using this product

OTC - WHEN USING SECTION

do not get into eyes. If contact occurs, rinse eyes thoroughly with water

Stop use and ask a 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 ■ rub hands vigorously until dry ■ children under 6 years of age should be supervised when using this product

Other Information

SPL UNCLASSIFIED SECTION

​■ store below 105°F (40°C) ■ may discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, propylene glycol, acrylates/c10-30 alkyl acrylates crosspolymer, isopropyl alcohol, aminomethylpropanol, isopropyl myristate, caprylyl glycol, phenoxyethanol, fragrance, tocopheryl acetate

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

Products#

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
20276-16720276-167-02, 20276-167-08, 20276-167-18

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
febab8b7-3d63-001d-e053-6294a90a25e6d3e6dcf6-786b-d4a5-e053-2995a90af62e2023-06-22WarningsExact identifier
spl id: febab8b7-3d63-001d-e053-6294a90a25e6
spl set id: d3e6dcf6-786b-d4a5-e053-2995a90af62e

Reported adverse events (FAERS/openFDA)#

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