SANIFOAM HAND SANITIZER

Manufacturer: AMERICAN CHEMICAL AND SANITARY SUPPLY INC
Effective date: 2024-05-09
Label type: HUMAN OTC DRUG LABEL
Version: 8
Source: full-release
Hydrated at: 2026-06-01 00:12:21

Label at a glance#

ProductSANIFOAM HAND SANITIZER

Active ingredientALCOHOL

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENT:

ALCOHOL (62% V/V)

OTC - PURPOSE SECTION

PURPOSE:

ANTIMICROBIAL

WARNINGS SECTION

FIRST AID:

EYES: AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE WITH WATER. CALL PHYSICIAN IF IRRITATION OR REDNESS DEVELOPS AND LASTS.

INGESTION: IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL OR CONTACT A POISON CNTROL CENTER IMMEDIATELY.

CONTAINER DISPOSAL: RINSE THREE TIMES WITH WATER. THEN OFFER FOR RECYCLING OR RECONDITIONING OR PUNCTURE AND DISPOSE OF IN A SANITARY LANDFILL OR BY INCARCERATION OR, IF ALLOWED BY STATE AND LOCAL AAUTHORITIES, BY BURNING. IF BURNED, STAY AWAY FROM SMOKE.

INDICATIONS & USAGE SECTION

USES: Hygienic disinfectant.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

FOR USE BY SERVICE PROFESSIONALS ONLY.

KEEP OUT OF REACH OF CHILDREN.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: WATER

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS:

POUR GEL INTO DISPENSER AND USE STRAIIGHT; DO NOT DILUTE. WET HANDS THOROUGHLY WITH PRODUCT AND ALLOW TO DRY WITHOUT WIPING. FOR EXTERNAL USE ONLY.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

soft touch plus copy

Drug Facts Box_Sanifoam Hand Sanitizer

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1491773	alcohol 62 % Medicated Liquid Soap	PSN	8
1491773	ethanol 0.62 ML/ML Medicated Liquid Soap	SCD	8
1491773	ethanol 62 % Medicated Liquid Soap	SY	8

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
50536-039-01	2024-05-09	C162847	48780-1	1030e365-2e2e-111a-e063-dadaa90a10e2	AMERICAN CHEMICAL AND SANITARY SUPPLY - SANIFOAM HAND SANITIZER (50536-039)
50536-039-01	2024-01-30	C162847	48780-1	1030e365-2e2e-111a-e063-dadaa90a10e2	AMERICAN CHEMICAL AND SANITARY SUPPLY - SANIFOAM HAND SANITIZER (50536-039)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
50536-039-01	SANIFOAM HAND SANITIZER	3785 mL in 1 JUG	LOTION	3785		8

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
50536-039	SANIFOAM HAND SANITIZER (ALCOHOL) LOTION [AMERICAN CHEMICAL AND SANITARY SUPPLY INC]	8	Legacy NDC, 1 package rows	20240511_9879a4c2-28d7-410f-b895-2a43dad684c2.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
ALCOHOL	ACTIVE INGREDIENT	3K9958V90M	4
ALCOHOL	ACTIVE MOIETY	3K9958V90M	4
WATER	INACTIVE INGREDIENT	059QF0KO0R	4

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

SANIFOAM HAND SANITIZER
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
50536-039	50536-039-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB

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
180ca979-0142-ae9d-e063-6294a90ae8c9			9879a4c2-28d7-410f-b895-2a43dad684c2	2024-05-09	Warnings	Exact identifier spl id: 180ca979-0142-ae9d-e063-6294a90ae8c9 spl set id: 9879a4c2-28d7-410f-b895-2a43dad684c2

Reported adverse events (FAERS/openFDA)#

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