BROOKSTONE ALOE ADVANCED FOAMING HAND SANITIZER- benzalkonium chloride solution

Brookstone Aloe Advanced Foaming Hand Sanitizer by

Drug Labeling and Warnings

Brookstone Aloe Advanced Foaming Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Argento sc by sicura inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Benzalkonium Chloride 0.13%

PURPOSE

Purpose: 

Antibacterial

Use

Decreases bacteria on skin that could cause diseases

Recommended for repeated use

Warnings

For external use on hands only.

When using this product

When using this product, keep out of eyes. In case of contact with eyes, flush thoroughly with water

Do not ingest or inhale

Avoid contact with broken skin

Stop use and ask a doctor

if irrigation and 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 immediately

Directions

• Spread product on hands thoroughly and allow to dry, do not wipe off
• For children under 6, use only under adult supervision
• Not recommended for use with infants

Other information

Do not store above 105F (40.6C)

May discolor some fabrics

Harmful to plastics and wood finished

Inactive ingredients

Water, Sodium lauroamphoacetate, Cocamidopropylamine oxide, Cocamidopropyl betaine, Glycerin, Olea europaea (olive) leaf extract, Polyminopropyl biguanide, Citric acid, Disodium EDTA, Benzophenone-3, Methylchloroisothiazolinone, Methylisothiazolinone, Fragrance, Cetylpyridinium chloride, Blue 1 (CI42090)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BROOKSTONE ALOE ADVANCED FOAMING HAND SANITIZER 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77731-089
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
SODIUM LAUROAMPHOACETATE (UNII: SLK428451L)
COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
GLYCERIN (UNII: PDC6A3C0OX)
OLEA EUROPAEA LEAF (UNII: MJ95C3OH47)
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
DISODIUM HEDTA (UNII: KME849MC7A)
BENZOPHENONE (UNII: 701M4TTV9O)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77731-089-01	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/17/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/17/2020

Labeler - Argento sc by sicura inc. (168718778)