FOAMING HAND SANITIZER REFILL MOISTURIZING ALOE- benzalkonium chloride liquid
Bocks Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Foaming Hand Sanitizer Refill (Moisturizing Aloe)

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Uses

• hand sanitizer that helps decrease bacteria on the skin
• recommend for repeated use

Warnings

For external use only, do not use in ears, mouth, or eyes.

When using this product

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

Stop use and ask a doctor

if irritation or redness develops, or if condition persists for more than 72 hours.

Keep out of reach of children

Children should be supervised when using this product.

Directions

• pour liquid into a foaming dispenser
• pump a small amount of foam into palm of hand
• spread thoroughly on both hands
• rub hands together until dry

Inactive Ingredients

Aloe Juice, Citric Acid, Dimonium Chloride Cocoamidopropyl Hydroxyethyldimonium Chloride, Hydroxypropyl Bis-Hydroxyethyldimonium Chloride,Rose Ether, Sodium Citrate, Water

Package Labeling: 473ml

Bottle3

Package Labeling: 946ml

Bottle4

FOAMING HAND SANITIZER REFILL MOISTURIZING ALOE
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:81527-001
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
HYDROXYPROPYL BIS-HYDROXYETHYLDIMONIUM CHLORIDE (UNII: 1EO3O1X7HG)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:81527-001-16	473 mL in 1 CARTON; Type 0: Not a Combination Product	02/01/2021
2	NDC:81527-001-32	946 mL in 1 CARTON; Type 0: Not a Combination Product	02/01/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	02/01/2021

Labeler - Bocks Inc (082200343)