LOVE CARD

Manufacturer: Shelko Electronics Co.,Ltd.
Effective date: 2022-11-27
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:51:53

Label at a glance#

ProductLOVE CARD

Active ingredientBENZALKONIUM

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

benzalkonium

INACTIVE INGREDIENT SECTION

Water

OTC - PURPOSE SECTION

Antibacterial, anti-fungal, indoor air purification, humidity control and insect repellent, sick house syndrome, formaldehyde neutralization, forest bathing effect and stress relief, sterilization deodorization, hand sanitizer, super bacteria inhibition, sleep effect, house mite avoidance, allergy and atopy improvement

WARNINGS SECTION

Do not drink.
Beware of fire.
Keep out of reach of children.
Avoid direct sunlight.
Do not use directly on the skin

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out of Reach of Children

DOSAGE & ADMINISTRATION SECTION

for topical use only

INDICATIONS & USAGE SECTION

Dilute with 5g of oil in 500ml of water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
82419-0003-1	2024-01-30	C162847	48780-1	1030e365-1426-111a-e063-dadaa90a10e2	ee80f146-8201-a5cb-e053-2a95a90a3abc

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
82419-0003-1	LOVE CARD	5 mL in 1 POUCH	LIQUID	5		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
82419-0003	LOVE CARD (BENZALKONIUM) LIQUID [SHELKO ELECTRONICS CO.,LTD.]	1	Legacy NDC, 1 package rows	20221128_ee80f146-8201-a5cb-e053-2a95a90a3abc.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

LOVE CARD
benzalkonium
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
82419-0003	82419-0003-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BENZALKONIUM	7N6JUD5X6Y	ACTIB
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
ee80f146-8202-a5cb-e053-2a95a90a3abc			ee80f146-8201-a5cb-e053-2a95a90a3abc	2022-11-27	Warnings	Exact identifier spl id: ee80f146-8202-a5cb-e053-2a95a90a3abc spl set id: ee80f146-8201-a5cb-e053-2a95a90a3abc

Reported adverse events (FAERS/openFDA)#

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