Dynamic Hand Sanitizing Wipes

Manufacturer: Milky Way International Trading Corp | Kangna (Zhejiang) Medical Supplies Co., Ltd.
Effective date: 2022-02-08
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:48:08

Label at a glance#

ProductDynamic Hand Sanitizing Wipes

Active ingredientBENZALKONIUM CHLORIDE

Label structure6 sections

Dosage and administration

Open lid, gently pull back resealable label, pull out wipes to wipe hands throughly for 30 seconds. Reseal back after use to prevent moisture from evaporating.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Purpose

OTC - PURPOSE SECTION

Antiseptic

USE

INDICATIONS & USAGE SECTION

●For hand sanitizing to decrease bacteria on the skin.
●Apply topically to the skin to help prevent cross contamination.
● Recommended for repeated use.
●Dries in seconds.

Warning

WARNINGS SECTION

For external use only.
Do not use in or contact the eyes.
Stop use and ask a doctor if too much skin irritation or
sensitivity develops or increases.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children. If swallowed, contact medical help or call Poison Control immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Open lid, gently pull back resealable label, pull out wipes to wipe
hands throughly for 30 seconds.
Reseal back after use to prevent moisture from evaporating.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Phenoxyethanol, DMDM Hydantoin, Polysorbate 20,
Ethylparaben, Methylparaben, Disodium EDTA, Sodium Citrate,
Cetylpyridinium Chloride.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

321

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1812737	benzalkonium Cl 0.3 % Medicated Pad	PSN	2
1812737	benzalkonium chloride 3 MG/ML Medicated Pad	SCD	2
1812737	benzalkonium chloride 0.3 % Medicated Wipe	SY	2
1812737	benzalkonium chloride 0.3 % Topical Cloth	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79203-001-01	2025-01-30	C162847	48780-1	d6a99b39-dea4-a426-e053-dadaa90af4c2	79203-001 Dynamic hand sanitizing wipes 0.3% Benzalkonium Chloride
79203-001-02	2025-01-30	C162847	48780-1	d6a99b39-dea4-a426-e053-dadaa90af4c2	79203-001 Dynamic hand sanitizing wipes 0.3% Benzalkonium Chloride
79203-001-01	2022-02-08	C162847	48780-1	d6a99b39-dea4-a426-e053-dadaa90af4c2	79203-001 Dynamic hand sanitizing wipes 0.3% Benzalkonium Chloride
79203-001-02	2022-02-08	C162847	48780-1	d6a99b39-dea4-a426-e053-dadaa90af4c2	79203-001 Dynamic hand sanitizing wipes 0.3% Benzalkonium Chloride
79203-001-01	2022-01-28	C162847	48780-1	d6a99b39-dea4-a426-e053-dadaa90af4c2	79203-001 Dynamic hand sanitizing wipes 0.3% Benzalkonium Chloride
79203-001-02	2022-01-28	C162847	48780-1	d6a99b39-dea4-a426-e053-dadaa90af4c2	79203-001 Dynamic hand sanitizing wipes 0.3% Benzalkonium Chloride

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
79203-001-01	Dynamic Hand Sanitizing Wipes	50 in 1 BAG	CLOTH	50	2
79203-001-01	Dynamic Hand Sanitizing Wipes	5.4 g in 1 PATCH	CLOTH	5.4	2
79203-001-02	Dynamic Hand Sanitizing Wipes	5.4 g in 1 PATCH	CLOTH	5.4	2
79203-001-02	Dynamic Hand Sanitizing Wipes	25 in 1 BAG	CLOTH	25	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79203-001	DYNAMIC HAND SANITIZING WIPES (BENZALKONIUM CHLORIDE) CLOTH [MILKY WAY INTERNATIONAL TRADING CORP]	2	Legacy NDC, 4 package rows	20220209_ab62043e-7d0c-171c-e053-2995a90a9497.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

Dynamic Hand Sanitizing Wipes
Benzalkonium Chloride
WATER
DISODIUM EDTA-COPPER
POLYSORBATE 20
PHENOXYETHANOL
SODIUM CITRATE
BENZALKONIUM
CETYLPYRIDINIUM CHLORIDE
ETHYLPARABEN
DMDM HYDANTOIN
METHYLPARABEN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79203-001	79203-001-01, 79203-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
DISODIUM EDTA-COPPER	6V475AX06U	IACT
POLYSORBATE 20	7T1F30V5YH	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
SODIUM CITRATE	1Q73Q2JULR	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
CETYLPYRIDINIUM CHLORIDE	D9OM4SK49P	IACT
ETHYLPARABEN	14255EXE39	IACT
DMDM HYDANTOIN	BYR0546TOW	IACT
METHYLPARABEN	A2I8C7HI9T	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
d77c7c9e-edce-a011-e053-2995a90a3ce6			ab62043e-7d0c-171c-e053-2995a90a9497	2022-02-08	Warnings	Exact identifier spl id: d77c7c9e-edce-a011-e053-2995a90a3ce6 spl set id: ab62043e-7d0c-171c-e053-2995a90a9497

Reported adverse events (FAERS/openFDA)#

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