Multi-purpose Antibacterial Wet Wipes

Manufacturer: Supreme Premium Products,Inc.
Effective date: 2020-07-10
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 23:22:01

Label at a glance#

ProductMulti-purpose Antibacterial Wet Wipes

Active ingredientBENZALKONIUM CHLORIDE

Label structure13 sections

Dosage and administration

Open using a label attached, pull out the wipe, and then seal the opening by sticking back the label to prevent the wipe from drying out.

Storage and handling

The expiry date is stated on the packaging, Store at -20℃ to +30℃,away from sunlight.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial Agent

Use

INDICATIONS & USAGE SECTION

Decreases bacteria on skin.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

Do not use if you are allergic to any of the ingredients.

OTC - WHEN USING SECTION

Using this product do not get into eyes. lf contact occurs, rinse thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Open using a label attached, pull out the wipe, and then seal the opening by sticking back the label to prevent the wipe from drying out.

Other information

STORAGE AND HANDLING SECTION

The expiry date is stated on the packaging, Store at -20℃ to +30℃,away from sunlight.

Inactive ingredients

INACTIVE INGREDIENT SECTION

C12-14 Alkyl Dimethyl, Ethylbenzyl Ammonium Chloride, Alkyl Polyglucoside, Disodium EDTA, Propylene Glycol, Aqua.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label-15label-15-2

label-60label-60-2label-75

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79531-003-01	2025-12-30	C162847	48780-1	2cef2736-98f3-d83d-e063-dadaa90ab31f	aa1e94f8-d808-1ad7-e053-2a95a90a3f94
79531-003-02	2025-12-30	C162847	48780-1	2cef2736-98f3-d83d-e063-dadaa90ab31f	aa1e94f8-d808-1ad7-e053-2a95a90a3f94
79531-003-03	2025-12-30	C162847	48780-1	2cef2736-98f3-d83d-e063-dadaa90ab31f	aa1e94f8-d808-1ad7-e053-2a95a90a3f94
79531-003-01	2025-01-30	C162847	48780-1	2cef2736-98f3-d83d-e063-dadaa90ab31f	aa1e94f8-d808-1ad7-e053-2a95a90a3f94
79531-003-02	2025-01-30	C162847	48780-1	2cef2736-98f3-d83d-e063-dadaa90ab31f	aa1e94f8-d808-1ad7-e053-2a95a90a3f94
79531-003-03	2025-01-30	C162847	48780-1	2cef2736-98f3-d83d-e063-dadaa90ab31f	aa1e94f8-d808-1ad7-e053-2a95a90a3f94

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79531-003	MULTI-PURPOSE ANTIBACTERIAL WET WIPES (BENZALKONIUM CHLORIDE) CLOTH [SUPREME PREMIUM PRODUCTS,INC.]	1	Legacy NDC	20200711_aa1e94f8-d808-1ad7-e053-2a95a90a3f94.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Multi-purpose Antibacterial Wet Wipes
BENZALKONIUM CHLORIDE
N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM CHLORIDE (C12-C14)
DECYL GLUCOSIDE
WATER
BENZALKONIUM
PROPYLENE GLYCOL
EDETATE DISODIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79531-003	79531-003-01, 79531-003-02, 79531-003-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM CHLORIDE (C12-C14)	G258TFN61X	IACT
DECYL GLUCOSIDE	Z17H97EA6Y	IACT
WATER	059QF0KO0R	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
PROPYLENE GLYCOL	6DC9Q167V3	IACT
EDETATE DISODIUM	7FLD91C86K	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
472862de-ca58-ecd0-e063-6394a90afd26			aa1e94f8-d808-1ad7-e053-2a95a90a3f94	2025-12-30	Warnings	Exact identifier spl set id: aa1e94f8-d808-1ad7-e053-2a95a90a3f94

Reported adverse events (FAERS/openFDA)#

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