Hand Sanitizer Wipes

Manufacturer
Southern Telecom, Inc.
Effective date
2025-06-05
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:03:38

Label at a glance#

ProductHand Sanitizer Wipes
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

• Unfold, and wipe hands thoroughly for about 30 seconds. • For children under 6, use only under adult supervision. • Not recommended for infants. • Dispose of wipe in trash after use. DO NOT flush.

Storage and handling

• Store at room temperature (66°F-77°F) • May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only, do not inhale or ingest.

Do not use in, or near eyes. In case of contact with eyes, rinse thoroughly with water.

Avoid contact with broken skin

Stop use and ask a doctor if irritation or rash develops and persists 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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

• Unfold, and wipe hands thoroughly for about 30 seconds.
• For children under 6, use only under adult supervision.
• Not recommended for infants.
• Dispose of wipe in trash after use. DO NOT flush.

Other information

STORAGE AND HANDLING SECTION

• Store at room temperature (66°F-77°F)
• May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Extract, Benzalkonium Chloride, Cetylpyridinium Chloride, Chamomilla Recutita (Matricaria) Flower Extract, Decyl Glucoside, Didecyldimonium Chloride, Glycerin, Water

SPL UNCLASSIFIED SECTION

Kills 99.99% of germs

With Aloe Moisturizer

Seal keeps wipes moist

1. Peel the seal carefully

2. Take out a wipe

3. Close properly and keep wipes moist

Cleanology

www.cleanologyproducts.com

Distributed by: Southern Telecom, Inc.

5601 1st Avenue Brooklyn, NY 11220

Cleanology is a trademark of Southern Telecom, Inc.

Made in China

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hand Sanitizer WipesHand Sanitizer Wipes

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76546-002-05Hand Sanitizer Wipes50 in 1 CONTAINERCLOTH504
76546-002-10Hand Sanitizer Wipes10 in 1 PACKAGECLOTH104
76546-002-15Hand Sanitizer Wipes150 in 1 CONTAINERCLOTH1504
76546-002-50Hand Sanitizer Wipes50 in 1 PACKAGECLOTH504
76546-002-80Hand Sanitizer Wipes80 in 1 BAGCLOTH804

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76546-00276546-002-15, 76546-002-05, 76546-002-50, 76546-002-10, 76546-002-80

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
Hand Sanitizer WipesALCOHOLSouthern Telecom, Inc.a6d06b25-735a-73c1-e053-2995a90a8b3c2025-06-05WarningsExact identifier
ndc (package): 76546-002-15
ndc (package): 76546-002-80
ndc (package): 76546-002-05
ndc (package): 76546-002-10
ndc (package): 76546-002-50
ndc (product): 76546-002
ndc11 (package): 76546000215
ndc11 (package): 76546000280
ndc11 (package): 76546000210
ndc11 (package): 76546000250
ndc11 (package): 76546000205
spl id: 65b666bf-2a02-44fd-a71d-696b6619130e
spl set id: a6d06b25-735a-73c1-e053-2995a90a8b3c

Reported adverse events (FAERS/openFDA)#

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