COMPANION Foaming Antibacterial Hand Soap

Companion by

Drug Labeling and Warnings

Companion by is a Otc medication manufactured, distributed, or labeled by Preserve International. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

COMPANION- companion antibacterial hand soap liquid 
Preserve International

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COMPANION
Foaming Antibacterial Hand Soap

DRUG FACTS
Active ingredients

Benzalkonium Chloride 0.13%....................Antibacterial

PURPOSE

Antimicrobial

USES

For hand washing to minimize bacteria on the skin.

WARNINGS

For External use only.

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.

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS

• Pump foam into dry hands.
• Lather with water for atleast 20 seconds.
• Rinse and pat dry.

OTHER INFORMATION

Store below 110°F (43°C). 

INACTIVE INGREDIENTS

Water, Xanthan Gum, Glycerin, Sodium Lauryl Eather Sulfate, Alkylpolyglycoside, Cocamidopropyl Betaine, Citric Acid, Sodium Citrate, Tetrasodium Ethylenediamine Tetraacetate, Sodium Benzoate, Waterfall Mist, Blue #1, Yellow #5.

COMPANION

Foaming Antibacterial Hand Soap

• Kills 99.9% of common bacteria
• Moisturizing Formula
• Light Fresh Scent

NET CONTENTS: 16.9 oz. (750 ml)

Item No.: 4900912/6

​Manufactured By:

Preserve International, a wholly-owned subsidiary of Neogen ®

944 Nandino Blvd. Lexington, KY 40511 USA

800-477-8201 (USA/Canada) or 859-254-1221 L7018-0920

COMPANION 
companion antibacterial hand soap liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60648-7200
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	2.9 mg  in 1 L

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
XANTHAN GUM (UNII: TTV12P4NEE)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
EDETATE SODIUM (UNII: MP1J8420LU)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60648-7200-1	0.75 L in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	11/04/2020	09/05/2025
2	NDC: 60648-7200-2	3.78 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/04/2020	09/05/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	11/04/2020	09/05/2025

Labeler - Preserve International (808154199)

Registrant - Preserve International (808154199)

Establishment
Name	Address	ID/FEI	Business Operations
Preserve International		808154199	manufacture(60648-7200) , api manufacture(60648-7200)

Revised: 12/2024

Document Id: 296a5d5a-9d2b-fef9-e063-6294a90a1b08

34390-5

Set id: f60ebf07-ba25-45f6-a381-e4d439dab0f9

Version: 4

Effective Time: 20241216