PURGO AF- benzalkonium chloride liquid

Purgo AF Gel by

Drug Labeling and Warnings

Purgo AF Gel by is a Otc medication manufactured, distributed, or labeled by Environmental Manufacturing Solutions, LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.13% v/v Antimicrobial

USES

Hand Sanitizer to help reduce bacteria on the skin

Warnings

For External Use Only.
Do not use in eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if skin irritation develops. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Directions

Apply to hands liberally. Gently massage into skin until absorbed. Supervise children in the use of this product.

QUESTIONS

Questions/Comments? Call toll free 1-800-510-8812

Other Ingredients

Water, Glycerine, Citric Acid, Lemongrass Oil

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.

PURPOSE

Hand Sanitizer to help reduce bacteria on the skin

Purgo AF 59mL package label

Purgo AF 295mL label

Package Label 3.785 L

Package label 9.46 L

Package Label 208 L

Package Label 1040L

Package Label Hand Sanitizer wipes

INGREDIENTS AND APPEARANCE

PURGO AF 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74869-420
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1274 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	99.02 g  in 100 g
EAST INDIAN LEMONGRASS OIL (UNII: UP0M8M3VZW)	0.04435 g  in 100 g
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)	0.15 g  in 100 g
GLYCERIN (UNII: PDC6A3C0OX)	0.63 g  in 100 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74869-420-02	59 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/09/2020
2	NDC: 74869-420-10	295 g in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/09/2020
3	NDC: 74869-420-11	3785 g in 1 JUG; Type 0: Not a Combination Product	04/09/2020
4	NDC: 74869-420-25	9460 g in 1 JUG; Type 0: Not a Combination Product	04/09/2020
5	NDC: 74869-420-55	208000 g in 1 DRUM; Type 0: Not a Combination Product	04/09/2020
6	NDC: 74869-420-27	1040000 g in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK; Type 0: Not a Combination Product	04/09/2020
7	NDC: 74869-420-40	320 g in 1 CONTAINER; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug	04/09/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/09/2020

Labeler - Environmental Manufacturing Solutions, LLC. (031863249)

Establishment
Name	Address	ID/FEI	Business Operations
Environmental Manufacturing Solutions, LLC.		031863249	manufacture(74869-420)