Luck-Lady Alcohol Wipes

Manufacturer: Dong Hiep Trading and Investment Co., Ltd
Effective date: 2020-08-12
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:24:27

Label at a glance#

ProductLuck-Lady Alcohol Wipes

Active ingredientBENZALKONIUM CHLORIDE, ALCOHOL

Label structure11 sections

Storage and handling

• Store between 15-30°C (59-86°F). • Avoid freezing and excessive heat above 40°C (104°F).

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/w

Benzalkonium Chloride <1% w/w

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

Used for antibacterial hand skin, prevent bacteria.

WARNINGS SECTION

For external use only. Flammable. Keep away from fire.

OTC - DO NOT USE SECTION

• Keep away from fire.
• Do not wipe your eyes.
• Do not throw into the toilet (not soluble in water).

OTC - WHEN USING SECTION

• Please wait until the alcohol has completely evaporated after wiping.
• Before use, check whether the packaging is intact. Do not use if it is damaged.

OTC - STOP USE SECTION

Stop use and ask a doctor for those with alcohol allergy or sensitive skin.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

STORAGE AND HANDLING SECTION

• Store between 15-30°C (59-86°F).
• Avoid freezing and excessive heat above 40°C (104°F).

INACTIVE INGREDIENT SECTION

Purified water, Cocamidopropyl PG-Dimonium Chloride Phosphate,
Stearyldimoniumhydroxypropyl Laurylglucosides Chloride

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1 piece inner package

Luck-Lady Alcohol Wipes_package50 pieces package

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2381635	benzalkonium chloride 0.1 % / ethanol 75 % Medicated Pad	PSN	1
2381635	benzalkonium chloride 1 MG/ML / ethanol 0.75 ML/ML Medicated Pad	SCD	1
2381635	benzalkonium chloride 0.1 % / ethanol 75 % Medicated Pad	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79366-104-01	2022-01-28	C162847	48780-1	d6a99b39-92ff-a426-e053-dadaa90af4c2	aba20198-e344-f179-e053-2a95a90ac5f8
79366-104-50	2022-01-28	C162847	48780-1	d6a99b39-92ff-a426-e053-dadaa90af4c2	aba20198-e344-f179-e053-2a95a90ac5f8

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
79366-104-01	Luck-Lady Alcohol Wipes	5.2 g in 1 PATCH	CLOTH	5.2	1
79366-104-01	Luck-Lady Alcohol Wipes	50 in 1 PACKET	CLOTH	50	1
79366-104-50	Luck-Lady Alcohol Wipes	260 g in 1 POUCH	CLOTH	260	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79366-104	LUCK-LADY ALCOHOL WIPES (75% ALCOHOL WIPES) CLOTH [DONG HIEP TRADING AND INVESTMENT CO., LTD]	1	Legacy NDC, 3 package rows	20200812_aba20198-e344-f179-e053-2a95a90ac5f8.zip

Products#

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

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

Luck-Lady Alcohol Wipes
75% Alcohol wipes
BENZALKONIUM CHLORIDE
BENZALKONIUM
WATER
ALCOHOL
STEARYLDIMONIUMHYDROXYPROPYL LAURYLGLUCOSIDES CHLORIDE
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79366-104	79366-104-01, 79366-104-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB
STEARYLDIMONIUMHYDROXYPROPYL LAURYLGLUCOSIDES CHLORIDE	ONN0OB7U86	IACT
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE	H2KVQ74JM4	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
aba20198-e345-f179-e053-2a95a90ac5f8			aba20198-e344-f179-e053-2a95a90ac5f8	2020-08-12	Warnings	Exact identifier spl id: aba20198-e345-f179-e053-2a95a90ac5f8 spl set id: aba20198-e344-f179-e053-2a95a90ac5f8

Reported adverse events (FAERS/openFDA)#

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