PACIFIC BLUE ULTRA FOAMING FRAGRANCE FREE- ethyl alcohol solution

Pacific Blue Ultra Foaming by

Drug Labeling and Warnings

Pacific Blue Ultra Foaming by is a Otc medication manufactured, distributed, or labeled by Georgia-Pacific Consumer Products LP, Vi-Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Uses

To decrease bacteria on the skin that could cause disease

Recommended for repeated use

Warnings

FLAMMABLE, keep away from fire and flame

For external use only

When using this product

do not use in or near eyes   

Stop use and ask a doctor

if irritation or redness develops.  If condition persists for more than 72 hours consult a doctor.

Keep out of reach of children.

If swallowed, seek immediate medical attention or call a poison control center.

Directions

Wet hands thoroughly with product and allow to dry without wiping.

Inactive ingredients

Water, Isopropyl Alcohol, PEG-12 Dimethicone, Glycerin, Caprylic/Capric Triglyceride, Isopropyl Myristate

Additional rear label text for manual dispensers

Pacific Blue Ultra Foam Hand Sanitizer Fragrance Free

Manufactured for Georgia-Pacific Consumer Products LP. Atlanta, GA 30303

Quesitons? Call 1-866-HELLOGP (435-5647)

or visit us online at www.gppro.com

(c) Georgia Pacific Consumer Products LP. All rights reserved.

alcohol permit SDS-MO-15036, DSP-MO-28, DSP-MO-34

43335-1 PRDRevA16 L0015800BA

Additional rear label text for automatic dispensers

Pacific Blue Ultra Automated Foam Hand Sanitizer Fragrance Free

Sku 43337

Manufactured for Georgia-Pacific Consumer Products LP. Atlanta, GA 30303

Quesitons? Call 1-866-HELLOGP (435-5647)

or visit us online at www.gppro.com

(c) 2017 Georgia Pacific Consumer Products LP. All rights reserved.

alcohol permit SDS-MO-15036, DSP-MO-28, DSP-MO-34

43337-V1 PRDRevA L0017074BA

principal display panel

Foam Hand Sanitizer

1000 mL (33.8 FL OZ)

701.000/701AA

INGREDIENTS AND APPEARANCE

PACIFIC BLUE ULTRA FOAMING  FRAGRANCE FREE
ethyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54622-701
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PEG-12 DIMETHICONE (UNII: ZEL54N6W95)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54622-701-01	1000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	06/09/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/02/2016

Labeler - Georgia Pacific Consumer Products (806142217)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon, Inc.		790752542	manufacture(54622-701)