Mountain Air Scent FOAMING HAND SANITIZER

Manufacturer: K7 DESIGN GROUP INC | Bath Concept Cosmetics (Dongguan) Co., Ltd
Effective date: 2023-10-26
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:57:52

Label at a glance#

ProductMountain Air Scent FOAMING HAND SANITIZER

Active ingredientBENZALKONIUM CHLORIDE

Label structure7 sections

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

for hand-washing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

do not get into eyes.
if contact occurs, rinse eyes thoroughly with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation and redness develop

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

wet hands thoroughly with product and allow to dry without wiping.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Lauryl Glucoside, Polysorbate 20, PEG/PPG-17/6 Copolymer, Sodium Benzoate, PEG-40 Hydrogenated Caster Oil, Fragrance.

Package Labeling:473ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2

Package Labeling:236ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1020365	benzalkonium chloride 0.13 % Topical Foam	PSN	2
1020365	benzalkonium chloride 1.3 MG/ML Topical Foam	SCD	2
1020365	benzalkonium chloride 0.13 % Topical Foam	SY	2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
74177-040-08	Mountain Air Scent FOAMING HAND SANITIZER	236 mL in 1 POUCH	LIQUID	236		2
74177-040-16	Mountain Air Scent FOAMING HAND SANITIZER	473 mL in 1 POUCH	LIQUID	473		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
74177-040	MOUNTAIN AIR SCENT FOAMING HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [K7 DESIGN GROUP INC]	2	Current NDC, Legacy NDC, 2 package rows	20231026_c80fc58e-e2a5-4c8e-a211-abe81fc1231d.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

Mountain Air Scent FOAMING HAND SANITIZER
BENZALKONIUM CHLORIDE
WATER
LAURYL GLUCOSIDE
POLYSORBATE 20
PEG/PPG-17/6 COPOLYMER
SODIUM BENZOATE
POLYOXYL 40 HYDROGENATED CASTOR OIL
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74177-040	74177-040-08, 74177-040-16

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
LAURYL GLUCOSIDE	76LN7P7UCU	IACT
POLYSORBATE 20	7T1F30V5YH	IACT
PEG/PPG-17/6 COPOLYMER	P5QZM4T259	IACT
SODIUM BENZOATE	OJ245FE5EU	IACT
POLYOXYL 40 HYDROGENATED CASTOR OIL	7YC686GQ8F	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Mountain Air Scent FOAMING HAND SANITIZER	BENZALKONIUM CHLORIDE	K7 DESIGN GROUP INC	c80fc58e-e2a5-4c8e-a211-abe81fc1231d	2023-10-26	Warnings	Exact identifier ndc (package): 74177-040-08 ndc (package): 74177-040-16 ndc (product): 74177-040 ndc11 (package): 74177004016 ndc11 (package): 74177004008 spl id: 0897c92f-ad28-a897-e063-6394a90af29c spl set id: c80fc58e-e2a5-4c8e-a211-abe81fc1231d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.