OTC Medication Information: Garrison Home

GARRISON HOME- benzalkonium chloride liquid
HOME & BODY COMPANY

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.

Active ingredient

0.13% Benzalkonium Chloride

Purpose

Antibacterial

Use

Helps reduce bacterial on hands

Warning

For external use only.
When using this product do not use in or near the eyes.
In case of contact, rinse eyes throughly with water.

Keep out of reach of children

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

Directions

Dispense soap into dry hands, work into lather and scrub for at least 35 seconds. Then rinse off with water.

Inactive Ingredients

Water (Aqua), Lauramine Oxide, Cellulose Gum, Tetrasodium EDTA, Polysorbate 20, Fragrance, Glycerin, Cocamidopropyl Betaine

Product Label

21.5 purple
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refil purple
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refill black
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label
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GARRISON HOME
benzalkonium chloride liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:73746-036
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE 1.3 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
EDETATE SODIUM
POLYSORBATE 20
CARBOXYMETHYLCELLULOSE SODIUM
LAURAMINE OXIDE
COCAMIDOPROPYL BETAINE
GLYCERIN
WATER
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:73746-036-01 636 mL in 1 BOTTLE, PLASTIC None
2 NDC:73746-036-02 1893 mL in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 06/13/2020
Labeler — HOME & BODY COMPANY (081290720)
Registrant — HOME & BODY COMPANY (081290720)
Establishment
Name Address ID/FEI Operations
HOME & BODY COMPANY 081290720 manufacture (73746-036)

Revised: 07/2021 HOME & BODY COMPANY

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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