SM Clean Sterilization Tissue

Manufacturer: shammah pharm
Effective date: 2020-04-20
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:07:06

Label at a glance#

ProductSM Clean Sterilization Tissue

Active ingredientBENZALKONIUM CHLORIDE

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

benzalkonium chloride

OTC - PURPOSE SECTION

sterilization of hands, skin and so on

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

take appropriate amount on the hand, rub and dry well

WARNINGS SECTION

■ Flammable. Keep away from fire or flame.

■ For external use only.

■ Do not use in eyes.

■ lf swallowed, get medical help promptly.

■ Stop use, ask doctor lf irritation occurs.

■ Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

for external use only

INACTIVE INGREDIENT SECTION

purified water, sodium carbonate, non-woven fabric

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
75697-0003-1	2022-01-28	C162847	48780-1	d6a99b39-6fc7-a426-e053-dadaa90af4c2	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75697-0003-1	SM Clean Sterilization Tissue	460 g in 1 NOT APPLICABLE	LIQUID	460		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75697-0003	SM CLEAN STERILIZATION TISSUE (BENZALKONIUM CHLORIDE) LIQUID [SHAMMAH PHARM]	1	Legacy NDC, 1 package rows	20200421_a3b7feb0-3b8e-185e-e053-2995a90adffb.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

SM Clean Sterilization Tissue
benzalkonium chloride
SODIUM CARBONATE
WATER
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75697-0003	75697-0003-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SODIUM CARBONATE	45P3261C7T	IACT
WATER	059QF0KO0R	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
a3b801d1-d212-9ca5-e053-2a95a90abc07			a3b7feb0-3b8e-185e-e053-2995a90adffb	2020-04-20	Warnings	Exact identifier spl id: a3b801d1-d212-9ca5-e053-2a95a90abc07 spl set id: a3b7feb0-3b8e-185e-e053-2995a90adffb

Reported adverse events (FAERS/openFDA)#

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