SAFETY CLEAR ANTIBACTERIAL HAND- benzalkonium chloride liquid

Safety Clear Antibacterial Hand by

Drug Labeling and Warnings

Safety Clear Antibacterial Hand by is a Otc medication manufactured, distributed, or labeled by Blue Cross Laboratories, Inc, Blue Cross Laboratories. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient Purpose

Benzalkonium Chloride 0.13% Antibacterial

PURPOSE

Uses For hand washing to decrease bacteria on the skin

KEEP OUT OF REACH OF CHILDREN

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

WARNINGS

Warnings :

For external use only

when using this product

• Avoid contact with eyes. If case of eye contact, flush with water

INDICATIONS & USAGE

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

DOSAGE & ADMINISTRATION

Directions

Wet hands as needed
Lather vigorously for at least 15 seconds
Wash skin, rinse and dry thoroughly

INACTIVE INGREDIENT

Inactive ingredients Water(aqua), Sodium Laureth Sulfate, Sodium Chloride, DMDM Hydantoin, Fragrance, Citric Acid, Aliz Violet Dye

PRINCIPAL DISPLAY PANEL

Safety Antibacterial

Clear

Hand Soap

Cleans & Softens Hands

8 FL OZ (236 mL)

INGREDIENTS AND APPEARANCE

SAFETY CLEAR ANTIBACTERIAL HAND 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 22431-587
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
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
DMDM HYDANTOIN (UNII: BYR0546TOW)
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22431-587-01	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/25/2020
2	NDC: 22431-587-02	1180 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/25/2020
3	NDC: 22431-587-03	444 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/25/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/25/2020

Labeler - Blue Cross Laboratories, Inc (008298879)

Establishment
Name	Address	ID/FEI	Business Operations
Blue Cross Laboratories		008298879	manufacture(22431-587)