QELBY Hesperidin Patch

Manufacturer
JD LIFE SCIENCES CO., LTD
Effective date
2026-02-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:36:19

Label at a glance#

ProductQELBY Hesperidin Patch
Active ingredientSILICON
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Adhesive silicone gel

INACTIVE INGREDIENT SECTION

Purified water EZ water, Quantum Energy Powder, Hesperidin

OTC - PURPOSE SECTION

Skin conditions(Wounds, Pressure Ulcers), Muscle pain(Arthritis, Disc pain)

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

WARNINGS SECTION

∙Avoid contract with towels or friction while bathing or showering after application to prevent the patch from peeling off.

∙After application, detoxification effects may cause body impurities to be released and transferred onto clothing always wear undergarments over the applied area.

∙Temporary symptoms such as itching, tingling, or mild pain may occur after application and typically subside within a few days, depending on individual conditions.

INDICATIONS & USAGE SECTION

∙Apply the patch to localized areas of pain such as the neck, shoulders, back, arms, legs, knees, chest, abdominal or pelvic areas, etc.

∙Replace with a new patch after wearing it continuously for more than 7 days per application

∙The effect continues even during bathing or showering.

∙Follow the instructions provided on the QR code and in the product manual.

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87369-0001-1QELBY Hesperidin Patch1.2 g in 1 PATCHPATCH1.21

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87369-000187369-0001-1

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
NameUNIIKind
SILICONZ4152N8IUIACTIB
WATER059QF0KO0RIACT

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
5a1180c5-2b12-fbce-e063-6294a90a544349e2af07-a634-d1ea-e063-6394a90ae0f02026-08-27WarningsExact identifier
spl set id: 49e2af07-a634-d1ea-e063-6394a90ae0f0

Reported adverse events (FAERS/openFDA)#

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