Hand Sanitizer Gel

Manufacturer: Hamilton Sundstrand Corporation
Effective date: 2020-04-23
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 23:34:17

Label at a glance#

ProductHand Sanitizer Gel

Active ingredientALCOHOL

Label structure10 sections

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

Antimicrobial

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on skin.

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70% v/v

DOSAGE & ADMINISTRATION SECTION

Place enough product in your palm to thoroughly cover hands and rub hands together briskly until dry.

WARNINGS SECTION

Flammable. Keep Away from fire or flame.

For external use only.

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

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

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

OTHER SAFETY INFORMATION

Store below 110 ⁰F (43 ⁰ C)

May disolor certain fabrics or surfaces

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children under 6 years of age should be supervised when using this product.

INACTIVE INGREDIENT SECTION

water (aqua), carbomer, propanediol 2-amino methyl-1 propanol solution

RECENT MAJOR CHANGES SECTION

Dosage and Administration, Sequence 6, 4/2020

Indication and Usage, Sequence 2, 4/2020

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

237mL (8oz) NDC: 76705-001-01

76705 001 01 Label 8oz Pump

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
76705-001-01	2022-12-20	C162847	48780-1	d6a99b39-a3e6-a426-e053-dadaa90af4c2	Hand Sanitizer Gel
76705-001-01	2022-01-28	C162847	48780-1	d6a99b39-a3e6-a426-e053-dadaa90af4c2	Hand Sanitizer Gel

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

Hand Sanitizer Gel
Ethyl Alcohol
WATER
CARBOMER 940
ALCOHOL
AMINOMETHYLPROPANOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
76705-001	76705-001-01
61037-446

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
CARBOMER 940	4Q93RCW27E	IACT
ALCOHOL	3K9958V90M	ACTIB
AMINOMETHYLPROPANOL	LU49E6626Q	IACT

Source Document#

Source XML · Source PDF

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
f042f30f-9b8d-4942-e053-2a95a90aeff7			a3f9ca4c-5732-4a1a-e053-2a95a90a8065	2022-12-20	Warnings	Exact identifier spl set id: a3f9ca4c-5732-4a1a-e053-2a95a90a8065

Reported adverse events (FAERS/openFDA)#

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