Sipa Foam hand sanitizer with Moisturizers

Manufacturer: Tourel (Changsha)Hotel Supplies Co.,Ltd
Effective date: 2025-01-02
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 00:51:15

Label at a glance#

ProductSipa Foam hand sanitizer with Moisturizers

Active ingredientBENZALKONIUM CHLORIDE

Label structure12 sections

Dosage and administration

Pump a small amount of foam into palm of handRub thoroughly over all surfaces of both handsRub hands together briskly until dry

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.15 %

Purpose

OTC - PURPOSE SECTION

For hand sanitizing to decrease bacteria on the skin

Use

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

in or near the eyes in case of contact, rinse eyes thoroughly with water

When Using

OTC - WHEN USING SECTION

Pay attention to the method of use. do not touch eyes

Stop Use

OTC - STOP USE SECTION

if irritation or rashappears and lasts

Ask Doctor

OTC - ASK DOCTOR SECTION

if irritation or rashappears and lasts

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

lf swallowed, getmedical help or contact a Poison Control Center right

Directions

DOSAGE & ADMINISTRATION SECTION

Pump a small amount of foam into palm of handRub thoroughly over all surfaces of both handsRub hands together briskly until dry

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Didecyldimonium Chloride, Glycerin, PropyleneGlycol, Peg-10 Dimethicone, Peg-17 Dimethicone

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

0102

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1116729	benzalkonium chloride 0.15 % Topical Foam	PSN	2
1116729	benzalkonium chloride 1.5 MG/ML Topical Foam	SCD	2
1116729	benzalkonium chloride 0.15 % Topical Foam	SY	2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
83502-001-01	Sipa Foam hand sanitizer with Moisturizers	50 mL in 1 BOTTLE	LIQUID	50		2
83502-001-02	Sipa Foam hand sanitizer with Moisturizers	320 mL in 1 BOTTLE	LIQUID	320		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
83502-001	SIPA FOAM HAND SANITIZER WITH MOISTURIZERS (INSTANT HAND SANITIZER) LIQUID [TOUREL (CHANGSHA)HOTEL SUPPLIES CO.,LTD]	2	Current NDC, 2 package rows	20250109_fcb9fe65-837c-011b-e053-6294a90a4605.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

Sipa Foam hand sanitizer with Moisturizers
Instant hand sanitizer
BENZALKONIUM CHLORIDE
BENZALKONIUM
PEG-10 DIMETHICONE (220 CST)
PEG-175 DISTEARATE
DIDECYLDIMONIUM CHLORIDE
GLYCERIN
PROPYLENE GLYCOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
83502-001	83502-001-01, 83502-001-02

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
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
PEG-10 DIMETHICONE (220 CST)	287GF3Y3WC	IACT
PEG-175 DISTEARATE	96X9M8B71Y	IACT
DIDECYLDIMONIUM CHLORIDE	JXN40O9Y9B	IACT
GLYCERIN	PDC6A3C0OX	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
WATER	059QF0KO0R	IACT

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
Sipa Foam hand sanitizer with Moisturizers	INSTANT HAND SANITIZER	Tourel (Changsha)Hotel Supplies Co.,Ltd	fcb9fe65-837c-011b-e053-6294a90a4605	2025-01-02	Warnings	Exact identifier ndc (package): 83502-001-02 ndc (package): 83502-001-01 ndc (product): 83502-001 ndc11 (package): 83502000101 ndc11 (package): 83502000102 spl id: 2ab3d486-3c47-3530-e063-6394a90a3c35 spl set id: fcb9fe65-837c-011b-e053-6294a90a4605

Reported adverse events (FAERS/openFDA)#

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