PURGO AF- benzalkonium chloride liquid 
PURGO AF GEL- benzalkonium chloride gel 
Environmental Manufacturing Solutions, LLC.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Purgo AFHand Sanitizer

Active ingredient

Benzalkonium chloride 0.13% v/v

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?

Inactive ingredients

citric acid, glycerin, lemongrass oil, water

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 label

Purgo AF

Purgo AF -424 principal display

Purgo AF Eucalyptus

Purgo AF Gel Label

Purgo AF Gel 524 label

PURGO AF 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74869-420
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1274 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R) 99.02 g  in 100 g
EAST INDIAN LEMONGRASS OIL (UNII: UP0M8M3VZW) 0.04435 g  in 100 g
GLYCERIN (UNII: PDC6A3C0OX) 0.63 g  in 100 g
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) 0.15 g  in 100 g
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:74869-420-0259 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product04/09/2020
2NDC:74869-420-10295 g in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product04/09/2020
3NDC:74869-420-113785 g in 1 JUG; Type 0: Not a Combination Product04/09/2020
4NDC:74869-420-259460 g in 1 JUG; Type 0: Not a Combination Product04/09/2020
5NDC:74869-420-55208000 g in 1 DRUM; Type 0: Not a Combination Product04/09/2020
6NDC:74869-420-271040000 g in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK; Type 0: Not a Combination Product04/09/2020
7NDC:74869-420-40320 g in 1 CONTAINER; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug04/09/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E04/09/202012/01/2023
PURGO AF 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74869-424
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1274 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R) 98.7036 g  in 100 g
EUCALYPTUS OIL (UNII: 2R04ONI662) 0.1832 g  in 100 g
GLYCERIN (UNII: PDC6A3C0OX) 0.63 g  in 100 g
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) 0.15 g  in 100 g
POLYSORBATE 80 (UNII: 6OZP39ZG8H) 0.2058 g  in 100 g
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:74869-424-0259 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/15/2020
2NDC:74869-424-10295 g in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product06/15/2020
3NDC:74869-424-113785 g in 1 JUG; Type 0: Not a Combination Product06/15/2020
4NDC:74869-424-259460 g in 1 JUG; Type 0: Not a Combination Product06/15/2020
5NDC:74869-424-55208000 g in 1 DRUM; Type 0: Not a Combination Product06/15/2020
6NDC:74869-424-271040000 g in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK; Type 0: Not a Combination Product06/15/2020
7NDC:74869-424-40320 g in 1 CONTAINER; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug06/15/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E06/15/202001/19/2023
PURGO AF GEL 
benzalkonium chloride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74869-524
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1274 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R) 98.5316 g  in 100 g
EUCALYPTUS OIL (UNII: 2R04ONI662) 0.061 g  in 100 g
GLYCERIN (UNII: PDC6A3C0OX) 0.63 g  in 100 g
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) 0.15 g  in 100 g
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16) 0.5 g  in 100 g
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:74869-524-0259 g in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product10/09/2020
2NDC:74869-524-113785 g in 1 JUG; Type 0: Not a Combination Product10/09/2020
3NDC:74869-524-55208000 g in 1 DRUM; Type 0: Not a Combination Product10/09/2020
4NDC:74869-524-271040000 g in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK; Type 0: Not a Combination Product10/09/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E10/09/202001/27/2024
Labeler - Environmental Manufacturing Solutions, LLC. (031863249)
Establishment
NameAddressID/FEIBusiness Operations
Environmental Manufacturing Solutions, LLC.031863249manufacture(74869-424, 74869-420, 74869-524)

Revised: 1/2023
Document Id: f2a0632a-d6e8-101f-e053-2995a90ac6a9
Set id: a2dffcf7-a16c-bf6d-e053-2995a90a0309
Version: 8
Effective Time: 20230119
 
Environmental Manufacturing Solutions, LLC.