FDA.reportPublic FDA data

First Aid Only Instant Hand Sanitizer Gel

Manufacturer
Acme United Corporation
Effective date
2020-06-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:27:18

Label at a glance#

ProductFirst Aid Only Instant Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

put enough gel in your palm to cover your hands and rub hand together rapidly until dry ■ children under 6 years of age should be supervised when using this product

Storage and handling

■ store below 110°F {43°C) ■ may discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% w/w

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

.hand sanitizer to help reduce microbes on the skin

Warnings

WARNINGS SECTION

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

OTC - WHEN USING SECTION

When using this product, do not use in or near the eyes. If contact occurs, rinse thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if redness or irritation develops and persists for more than 72 hours.

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

put enough gel in your palm to cover your hands and rub hand together rapidly until dry

■ children under 6 years of age should be supervised when using this product

Other information

STORAGE AND HANDLING SECTION

■ store below 110°F {43°C)

■ may discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

carbomer, fragrance, glycerin, propylene glycol, silicone, triethanolamine, water (aqua)

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle LabelBottle Label60 mL NDC: 0924-0401-01

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0924-04010924-0401-01, 0924-0401-02, 0924-0401-03, 0924-0401-04, 0924-0401-05, 0924-0401-06
28691-0700

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
SILICONZ4152N8IUIIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
TROLAMINE9O3K93S3TKIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
GLYCERINPDC6A3C0OXIACT

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
2511e329-6efd-7199-e063-6394a90ac374a7a8a84d-d0ee-2881-e053-2a95a90a59c42024-10-22WarningsExact identifier
spl set id: a7a8a84d-d0ee-2881-e053-2a95a90a59c4

Reported adverse events (FAERS/openFDA)#

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