Reliable 118.401/118AE Foaming Hand Sanitizer

Foaming Hand Sanitizer by

Drug Labeling and Warnings

Foaming Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by VERITIV OPERATING COMPANY, Vi-Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

FOAMING HAND SANITIZER- benzalkonium chloride lotion 
VERITIV OPERATING COMPANY

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Reliable 118.401/118AE
Foaming Hand Sanitizer

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Use

to decrease bacteria on the skin

Warnings

for external use only: hands only

When using this product

• avoid contact with eyes.  If contact occurs, rinse eyes thoroughly with water.
• avoid contact with broken skin

Stop use and ask a doctor if

• if irritation and redness develop
• condition persists for more than 72 hours

Keep out of reach of children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center right away

Directions

• wet hands thoroughly with product and allow to dry without wiping
• for children under 6, use only under adult supervision
• not recommended for infants

Inactive ingredients

cetrimonium chloride, diglycerin, disodium cocoamphodiacetate, fragrance, glycerin, hydrochloric acid, methoxy PEG/PPG-7/3 aminopropyl dimethicone, sodium benzoate, tetrasodium EDTA, water

Rear label text

Distributed by

Veritiv Operating Company

Atlanta, GA 30328

reliablebrand.com

PRINCIPAL DISPLAY PANEL

ALCOHOL FREE FOAM HAND SANITIZER

Manual push style

1 L (33.8 FL OZ)

FOAMING HAND SANITIZER 
benzalkonium chloride lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71897-118
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
DIGLYCERIN (UNII: 3YC120743U)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROCHLORIC ACID (UNII: QTT17582CB)
METHOXY PEG/PPG-7/3 AMINOPROPYL DIMETHICONE (UNII: 4M7P1JZ2V2)
SODIUM BENZOATE (UNII: OJ245FE5EU)
EDETATE SODIUM (UNII: MP1J8420LU)
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71897-118-45	1000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/05/2020	12/13/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/05/2020	12/13/2020

Labeler - VERITIV OPERATING COMPANY (006989982)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091520	manufacture(71897-118)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(71897-118)

Revised: 10/2024

Document Id: 253a89dd-165c-ea75-e063-6294a90a0428

34390-5

Set id: 194147d6-3452-467a-818b-bfad761e09c0

Version: 4

Effective Time: 20241024