DGP HIGH PERFORMANCE HAND SANITIZER- ethyl alcohol gel

DGP High Performance Hand Sanitizer by

Drug Labeling and Warnings

DGP High Performance Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Dynamic Green Products, Inc., Packaging Service Co, Viking Chemical Company, Vertrauen Chemie Solutions Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl Alcohol 76%

Purpose

Hand & Skin Antiseptic

INDICATIONS & USAGE

Hand & Skin Antiseptic to help decrease pathogens (germs) on the skin

WARNINGS

For external use only

Flammable: Keep away from heat and flame

* Avoid contact with eyes. If contact occurs flush eyes thoroughly with clean and cool water

* Do not ingest or inhale

Stop use and ask a doctor

* If irritation or redness develops, and/or you have open wounds or serious burns.

Stop use

* If irritation or redness develops

* Have open wounds or serious burns

Keep out of reach of children

* If swallowed, get medical help or contact a Poison Control Center immediately

Directions

* Apply a small amount of hand sanitizer each use to clean and protect hands

* Work thoroughly onto hands and allow to dry without wiping

* Reapply as needed

Inactive ingredients

Ethyl Lactate, Glycerin, Tocopheryl Acetate (Vitamin E), Hydroxypropyl Cellulose, Fragrance

Principal Display Panel

DGP (R) High Performance Hand Sanitizer

Bio-based Antibacterial Formula

Vitamin E + Essential Oils

To open pumps, pinch safety lock and twist nozzle

To open refill, pull back tab to reveal pour hole

All ingredients are made in the USA

The packaging is sourced in the USA

The hand pump is non-domestic sourced

Distributed by:

Dynamic Green Products, Inc.

11757 Katy Fwy Ste 1300

Houston, TX 77079

For additional Product information: Call 855-BIO-OILS or visit www.dgpworks.com

(C) Dynamic Green Products Inc. All Rights Reserved

XX oz (zzzmL) NDC: 74631-001-xx

INGREDIENTS AND APPEARANCE

DGP HIGH PERFORMANCE HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74631-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	76 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ETHYL LACTATE (UNII: F3P750VW8I)
HYDROXYPROPYL CELLULOSE (110000 WAMW) (UNII: 5Y0974F5PW)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74631-002-34	24 in 1 CASE	04/28/2020
1	NDC: 74631-002-06	6 in 1 BOX
1	NDC: 74631-002-01	946 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
2	NDC: 74631-002-24	24 in 1 CASE	04/28/2020
2	NDC: 74631-002-16	6 in 1 BOX
2	NDC: 74631-002-02	946 mL in 1 BOTTLE; 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	04/28/2020

Labeler - Dynamic Green Products, Inc. (110949053)

Registrant - Dynamic Green Products, Inc. (110949053)

Establishment
Name	Address	ID/FEI	Business Operations
Packaging Service Co		008435950	pack(74631-002) , repack(74631-002)

Establishment
Name	Address	ID/FEI	Business Operations
Viking Chemical Company		025807272	analysis(74631-002) , manufacture(74631-002)

Establishment
Name	Address	ID/FEI	Business Operations
Vertrauen Chemie Solutions Inc		080251121	pack(74631-002) , repack(74631-002)