Alcohol Foaming Hand Sanitizer

Manufacturer: Cintas Corp. | Best Santizers, Inc
Effective date: 2020-03-25
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: legacy-cache
Hydrated at: 2026-08-01 23:38:57

Label at a glance#

ProductAlcohol Foaming Hand Sanitizer

Active ingredientALCOHOL

Label structure8 sections

Storage and handling

Other Information: Store below 110 F (43 C) May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Ethyl alcohol 62%

OTC - PURPOSE SECTION

Purpose

Antimicrobial

INDICATIONS & USAGE SECTION

Uses

For hand sanitizing to decrease bacteria on the skin

Recommended for repeated use

WARNINGS SECTION

Warnings

Flammable. Keep away from fire or flames.

For external use only.

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops, or if condition 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.

DOSAGE & ADMINISTRATION SECTION

Directions:

Wash hands with soap and water

Rinse with potable water

Pump a small amount of foam into palm of hand

Rub thoroughly over all surfaces of both hands

Rub hands together briskly until dry

STORAGE AND HANDLING SECTION

Other Information:

Store below 110 F (43 C)

May discolor certain fabrics or surfaces

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

DEA-C8-18 perfluoroalkylethyl phosphate, Glycereth-2 cocoate, Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sanis

Alcohol Foaming

Hand Sanitizer

800 ML / 27 FL OZ

container label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
42961-012-02	2020-03-25	C162847	48780-1	9d75b9d0-a3a5-f424-e053-dadaa90a57ce	Drug Facts
42961-012-06	2020-03-25	C162847	48780-1	9d75b9d0-a3a5-f424-e053-dadaa90a57ce	Drug Facts
42961-012-02	2020-01-31	C162847	48780-1	9d75b9d0-a3a5-f424-e053-dadaa90a57ce	Drug Facts
42961-012-06	2020-01-31	C162847	48780-1	9d75b9d0-a3a5-f424-e053-dadaa90a57ce	Drug Facts

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
ALCOHOL	ACTIVE INGREDIENT	3K9958V90M	1
ALCOHOL	ACTIVE MOIETY	3K9958V90M	1
DIETHANOLAMINE BIS(C8-C18 PERFLUOROALKYLETHYL)PHOSPHATE	INACTIVE INGREDIENT	4J55VM509S	1
GLYCERETH-2 COCOATE	INACTIVE INGREDIENT	JWM00VS7HC	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

Alcohol Foaming Hand Sanitizer
ALCOHOL
DIETHANOLAMINE BIS(C8-C18 PERFLUOROALKYLETHYL)PHOSPHATE
GLYCERETH-2 COCOATE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
42961-012	42961-012-02, 42961-012-06

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
ALCOHOL	3K9958V90M	ACTIB
DIETHANOLAMINE BIS(C8-C18 PERFLUOROALKYLETHYL)PHOSPHATE	4J55VM509S	IACT
GLYCERETH-2 COCOATE	JWM00VS7HC	IACT
WATER	059QF0KO0R	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
7ccea9ba-7922-4102-8373-92b7523a1c5c			a32ea050-ee33-4673-ad46-d641a864b8a9	2022-04-14	Warnings	Exact identifier spl set id: a32ea050-ee33-4673-ad46-d641a864b8a9

Reported adverse events (FAERS/openFDA)#

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