SANIMOR ALCOHOL-FREE FOAMING HAND SANITIZER- benzalkonium chloride liquid

SANIMOR ALCOHOL-FREE FOAMING HAND SANITIZER by

Drug Labeling and Warnings

SANIMOR ALCOHOL-FREE FOAMING HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Avmor. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Benzalkonium chloride, 0.13%

Purpose

Antimicrobial

Uses

For personal hand hygiene to help decrease bacteria on skin.

Warnings

For external use only.

When using this product

Avoid contact with eyes. Should this occur, flush eyes with water.

Stop use and consult a physician

If irritation or redness develop, or if condition persists 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

Pump a small amount of Foaming Hand Sanitizer into the palm of your hand.

Rub product onto hands and allow to dry.

 Inactive ingredients

Water (Aqua), Glycerin, Lauryldimethylamine Oxide.

PRINCIPAL DISPLAY PANEL

Sanimor

Alcohol Free

Foaming

Hand Sanitizer

1L 33.8 FL OZ

Sanimor

Alcohol Free

Foaming

Hand Sanitizer

250mL 8.4 FL OZ

INGREDIENTS AND APPEARANCE

SANIMOR ALCOHOL-FREE FOAMING HAND SANITIZER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63937-2364
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63937-2364-1	12 in 1 BOX	12/22/2016
1		250 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 63937-2364-2	4 in 1 BOX	12/22/2016
2		1000 mL in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC: 63937-2364-3	2 in 1 BOX	12/22/2016
3		4000 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	part333E	12/20/2016

Labeler - Avmor (202107827)

Establishment
Name	Address	ID/FEI	Business Operations
Avmor		202107827	manufacture(63937-2364) , label(63937-2364) , pack(63937-2364)