Hand Sanitizing Wipes

Manufacturer: Tropical Degil Cosmetics Industries LTD
Effective date: 2020-10-12
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:31:27

Label at a glance#

ProductHand Sanitizing Wipes

Active ingredientBENZALKONIUM CHLORIDE

Label structure12 sections

Dosage and administration

For adults and children 3 years and over, wipe hands and discard. Allow hands to air dry.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13% v/v

Purpose

OTC - PURPOSE SECTION

Hand Sanitizer, Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

if you are allergic to any of the ingredients

OTC - WHEN USING SECTION

When using this product do not use in or near the eyes. If contact occurs, rinse thoroughly with water.

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if irritation or redness develops and lasts 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

For adults and children 3 years and over, wipe hands and discard. Allow hands to air dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Alcohol Denatured, Aloe Barbadensis Leaf Extract, Benzoic Acid, Caprylyl/Capryl Glucoside, Citric Acid, Dehydroacetic Acid, Disodium EDTA, Fragrance, Glycerin, Phenoxyethanol, Polysorbate 20, Water

OTHER SAFETY INFORMATION

Other information Store in a cool dry place.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

25 wipes. 0.13% Benzalkonium Chloride

Front Panel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1038558	benzalkonium chloride 0.13 % Medicated Pad	PSN	2
1038558	benzalkonium chloride 1.3 MG/ML Medicated Pad	SCD	2
1038558	benzalkonium chloride 0.13 % Topical Cloth	SY	2
1038558	benzalkonium chloride 0.13 % Topical Swab	SY	2
1038558	benzalkonium chloride 0.13 GM per 100 GM Topical Pad	SY	2
1038558	benzalkonium chloride 0.13 GM per 100 GM Topical Swab	SY	2
1038558	benzalkonium chloride 1 ML per 750 ML Topical Swab	SY	2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
c6f86816-7da6-43ea-8c25-ac9758311cc5	Product name	1	20220118
252e11b6-1a9a-4283-a242-df2c129c496d	Product name	3	20170717

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
62685-219-01	2022-01-28	C162847	48780-1	d6a99b39-4908-a426-e053-dadaa90af4c2	Vish Hand Wipes
62685-219-02	2022-01-28	C162847	48780-1	d6a99b39-4908-a426-e053-dadaa90af4c2	Vish Hand Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
62685-219-01	Hand Sanitizing Wipes	180 g in 1 PACKET	CLOTH	180		2
62685-219-02	Hand Sanitizing Wipes	108 g in 1 PACKET	CLOTH	108		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62685-219	HAND SANITIZING WIPES (BENZALKONIUM CHLORIDE) CLOTH [TROPICAL DEGIL COSMETICS INDUSTRIES LTD]	2	Legacy NDC, 2 package rows	20201013_ae703347-ee78-41f0-e053-2a95a90a03fa.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

Hand Sanitizing Wipes
Benzalkonium Chloride
CITRIC ACID MONOHYDRATE
GLYCERIN
ALOE VERA LEAF
EDETATE DISODIUM
BENZALKONIUM
ALCOHOL
DEHYDROACETIC ACID
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE
BENZOIC ACID
PHENOXYETHANOL
POLYSORBATE 20
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
62685-219	62685-219-01, 62685-219-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
GLYCERIN	PDC6A3C0OX	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
EDETATE DISODIUM	7FLD91C86K	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
ALCOHOL	3K9958V90M	IACT
DEHYDROACETIC ACID	2KAG279R6R	IACT
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE	E00JL9G9K0	IACT
BENZOIC ACID	8SKN0B0MIM	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
POLYSORBATE 20	7T1F30V5YH	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
b180e4d0-3449-64d8-e053-2995a90aea4c			ae703347-ee78-41f0-e053-2a95a90a03fa	2020-10-12	Warnings	Exact identifier spl id: b180e4d0-3449-64d8-e053-2995a90aea4c spl set id: ae703347-ee78-41f0-e053-2a95a90a03fa

Reported adverse events (FAERS/openFDA)#

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