SIGNATURE SERIES ENRICHED FOAM ALCOHOL HAND SANITIZER- alcohol liquid

Signature Series Enriched Foam Alcohol Hand Sanitizer by

Drug Labeling and Warnings

Signature Series Enriched Foam Alcohol Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Cintas Corporation, Rubbermaid Commercial Products LLC, NWL Netherlands Production BV. 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 of 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), PEG-6 Caprylic Glycerides, Sodium Lactate, PEG-14M, Silica, Disodium Lauriminodipropionate Tocopheryl Phosphates, Phenoxyethanol, Benzoic Acid, Dehydroacetic Acid, PEG/PPG-25/25 Dimethicone, Shea Butteramidopropyl Betaine, Hexylene Glycol, Sodium Citrate, Lactic Acid

Questions?

1-800-347-9800 Mon.–Fri., 8 AM–5 PM EST.

PRINCIPAL DISPLAY PANEL - 500 mL Pouch Box

Rubbermaid®
Commercial Products

Enriched Foam Alcohol Hand Sanitizer

500 mL (16.9 FL. OZ. U.S.)

HAND SANITIZER

CiNTAS®
Signature Series®

INGREDIENTS AND APPEARANCE

SIGNATURE SERIES ENRICHED FOAM ALCOHOL HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42961-017
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
CAPRYLOCAPROYL POLYOXYLGLYCERIDES 6 (UNII: GO50W2HWO8)
Sodium Lactate (UNII: TU7HW0W0QT)
POLYETHYLENE OXIDE 600000 (UNII: 2126FD486L)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
Disodium Lauriminodipropionate Tocopheryl Phosphates (UNII: 0K5Y9U1P6M)
Phenoxyethanol (UNII: HIE492ZZ3T)
Benzoic Acid (UNII: 8SKN0B0MIM)
Dehydroacetic Acid (UNII: 2KAG279R6R)
PEG/PPG-25/25 Dimethicone (UNII: ND6MYD0T84)
Hexylene Glycol (UNII: KEH0A3F75J)
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42961-017-01	4 in 1 BOX	05/08/2020
1		500 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 NOT FINAL	part333A	05/08/2020

Labeler - Cintas Corporation (056481716)

Establishment
Name	Address	ID/FEI	Business Operations
Cintas Corporation		056481716	RELABEL(42961-017)

Establishment
Name	Address	ID/FEI	Business Operations
NWL Netherlands Production BV		489421698	MANUFACTURE(42961-017)