FIRST MARK ULTRA FOAMING ANTIBACTERIAL- benzalkonium chloride solution

FIRST MARK ULTRA FOAMING ANTIBACTERIAL by

Drug Labeling and Warnings

FIRST MARK ULTRA FOAMING ANTIBACTERIAL by is a Otc medication manufactured, distributed, or labeled by Performance Food Group. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium chloride 0.5%

Purpose

Antiseptic handwash

Uses

• for handwashing to decrease bacteria on the skin

Warning

For external use only

Do not use

• in eyes

When using the product

• if in eyes, rinse promptly and thoroughly with water
• discontinue use if irritation and redness develop

Stop use and ask a doctor if

• skin irritation or redness occurs for more than 72 hours

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• wet hands and apply foam
• scrub hands and forearms
• rinsethoroughly and dry

Other information

• for additional information, see Safety Data Sheet (SDS)
• for emergency medical information in USA and Canada, call (833) 571-1403

INACTIVE INGREDIENT

Inactive ingredients water (aqua), cocamine oxide, hexylene glycol, PEG-180, glycerin, cocamidopropyl PG-dimonium chloride phosphate,  phenoxyethanol, polyquaternium 7, myristamide DIPA, myristamine oxide, citric acid, methyl gluceth-20, glyceryl caprylate/carate, alcohol, PEG-12 dimethicone, potassium citrate, fragrance, blue 1

QUESTIONS

Questions? call 1-800-532-7732

Principal display panel and representative container

REORDER% 644084

1111218   778366   778366/7300/0521

FIRST MARK

ULTRA FOAMING ANTIBACTERIAL

HAND SOAP

Active Ingredient: Benzalkonium Chloride 0.5%

NDC: 51042-001-10

Made in the USA

DISTRIBUTED BY:

PERFORMANCE FOOD GROUP

12500 WEST CREEK PARKWAY

RICHMOND VIRGINIA 23238

INGREDIENTS AND APPEARANCE

FIRST MARK ULTRA FOAMING ANTIBACTERIAL 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51042-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
COCAMINE OXIDE (UNII: QWA2IZI6FI)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B)
GLYCERIN (UNII: PDC6A3C0OX)
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
MYRISTIC DIISOPROPANOLAMIDE (UNII: 17DN142CTK)
MYRISTAMINE OXIDE (UNII: J086PM3RRT)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
METHYL GLUCETH-20 (UNII: J3QD0LD11P)
GLYCERYL CAPRYLOCAPRATE (UNII: U72Q2I8C85)
ALCOHOL (UNII: 3K9958V90M)
PEG-12 DIMETHICONE (UNII: ZEL54N6W95)
POTASSIUM CITRATE (UNII: EE90ONI6FF)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51042-001-10	1250 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/29/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/12/2015

Labeler - Performance Food Group (127038714)