ALCOHOL FOAM HAND SANITIZER- alcohol liquid

Alcohol Foam Hand Sanitizer by

Drug Labeling and Warnings

Alcohol Foam Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Rubbermaid Commercial Products LLC, Rubbermaid Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Alcohol Denat. 75% (v/v)

Purpose

Antiseptic cleanser

Use

To decrease potentially harmful germs on skin.

Warnings

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

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

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

• Keep out of reach of children.
• If swallowed, do not induce vomiting, get medical attention.

READ MATERIAL SAFETY DATA SHEET BEFORE USING PRODUCT

Directions

Apply generously to hands. Rub hands together. Allow hands to dry. Repeat daily as necessary.

Inactive ingredients

Water (Aqua), Acrylates/Perfluorohexylethyl Methacrylate Copolymer, Perfluorohexylethyl Alcohol, Glycerin

Questions?

1-800-347-9800

Mon–Fri, 8 AM–5 PM EST.

SPL UNCLASSIFIED SECTION

Distributed by Rubbermaid-Winfield Inc.
1616 Wheat Rd. Winfield, KS 67156-533

PRINCIPAL DISPLAY PANEL - 1000 mL Pouch Box

Rubbermaid®
Commercial Products

Alcohol Foam Hand Sanitizer

INGREDIENTS AND APPEARANCE

ALCOHOL FOAM HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65321-041
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PEG-10 ACRYLATE/PERFLUOROHEXYLETHYL ACRYLATE COPOLYMER (UNII: D76Z87928N)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65321-041-01	4 in 1 BOX	09/01/2022	09/01/2025
1		1000 mL in 1 POUCH; Type 0: Not a Combination Product
2	NDC: 65321-041-02	4 in 1 BOX	09/01/2022	09/01/2025
2		1000 mL in 1 POUCH; Type 0: Not a Combination Product
3	NDC: 65321-041-03	4 in 1 BOX	09/01/2022	09/01/2025
3		1000 mL in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH DRUG	M004	09/01/2022	09/01/2025

Labeler - Rubbermaid Commercial Products LLC (049924368)

Establishment
Name	Address	ID/FEI	Business Operations
Rubbermaid Inc.		118572215	MANUFACTURE(65321-041)