PIONEER ECLIPSE TOUCHE FOAMING NON-ALCOHOL HAND SANITIZER- benzalkonium chloride solution

Pioneer Eclipse Touche Foaming Non-Alcohol Hand Sanitizer by

Drug Labeling and Warnings

Pioneer Eclipse Touche Foaming Non-Alcohol Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by CWGC LA Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

BENZALKONIUM CHLORIDE  0.13%

Purpose

Antibacterial

Uses

• For handwashing to reduce bacteria on the skin. Recommended for repeated use.

Warnings

For external use only

Avoid contact with eyes. In case of eye contact, flush eyes with water.

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

STOP USE

Stop use and ask a doctor if irritation or redness develops and persists.

Directions

• Apply foam sanitizer to hands.
• Rub over surfaces of both hands for 15 seconds.
• No rinsing required.

Inactive ingredients

Water, Propylene Glycol, Cocamidopropyl Betaine, Cocamine Oxide, Disodium EDTA, DMDM Hydantoin, Triethanolamine, Fragrance, FD&C Yellow No.5, FD&C Blue No.1.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PIONEER ECLIPSE TOUCHE FOAMING NON-ALCOHOL HAND SANITIZER 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70415-305
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
COCAMINE OXIDE (UNII: QWA2IZI6FI)
EDETATE DISODIUM (UNII: 7FLD91C86K)
DMDM HYDANTOIN (UNII: BYR0546TOW)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70415-305-01	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/04/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/04/2017

Labeler - CWGC LA Inc. (034967904)