Snugell-QUANZHOU Spray 473 mL

Manufacturer
SNUGELL LLC | QUANZHOU AIWINA HYGIENE PRODUCTS CO.,LTD
Effective date
2024-12-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 20:46:45

Label at a glance#

ProductSnugell
Active ingredientBENZALKONIUM CHLORIDE
Label structure14 sections

Dosage and administration

Spray over the desired skin surface area and rub thoroughly. No rinse is required. Children under 6 years of age should be supervised when using this product.

Storage and handling

.Avoid freezing and store below 110F (43 C). Dispose the empty can in a recycle bin.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

in children less than 2 months of age
near eyes or on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.


if swallowed, get medical help or contact a poison control center right away at 800-222-1222.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

Spray over the desired skin surface area and rub thoroughly. No rinse is required.

Children under 6 years of age should be supervised when using this product.

OTC - QUESTIONS SECTION

Call 1-844-451-6555

Other information

STORAGE AND HANDLING SECTION

.Avoid freezing and store below 110F (43 C).

Dispose the empty can in a recycle bin.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe barbadensis leaf extract, butylene glycol, chamomilla recutita (matricaria) extract, grape seed extract, purified water.

SPL UNCLASSIFIED SECTION

Leaves No Chemical Residue

Alcohol-Free

Antiseptic Spray

with Aloe Vera

KILLS 99% OF GERMS AND BACTERIA

Distributed by:
Snugell, LLC
Miami, FL 33015
www.snugell.com

MADE IN CHINA

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

473 mL NDC: 82621-111-11473 mL NDC: 82621-111-11

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82621-111-112024-12-13C16284748780-10191ceaa-68d5-198a-e063-dbdaa90aec3eSnugell-QUANZHOU Spray 473 mL
82621-111-112023-07-28C16284748780-10191ceaa-68d5-198a-e063-dbdaa90aec3eSnugell-QUANZHOU Spray 473 mL

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82621-111SNUGELL (SANITIZING SPRAY) SPRAY [SNUGELL LLC]2Legacy NDC20241215_dbbcfc17-4021-4f64-e053-2a95a90a53ef.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82621-11182621-111-11

Ingredients#

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

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

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4ffb50e5-6163-7027-e063-6394a90ad515dbbcfc17-4021-4f64-e053-2a95a90a53ef2026-04-21WarningsExact identifier
spl set id: dbbcfc17-4021-4f64-e053-2a95a90a53ef

Reported adverse events (FAERS/openFDA)#

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