Pain Relieving Patch - DW SUPPORT LLC | Henan Kangdi Medical Devices Co. Ltd

Manufacturer
DW SUPPORT LLC | Henan Kangdi Medical Devices Co. Ltd
Effective date
2026-08-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-09-04 01:01:09

Label at a glance#

ProductTERAPIA DE DIA Y NOCHE
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE, CAPSAICIN
Label structure7 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and older:
Clean and dry affected area. Remove patch from film and apply to skin.
Apply to affected area no more than 3 to 4 times daily.
Remove patch from skin after at most 8 hours.
Children under 12 years of age:
Consult a doctor.

Warnings

WARNINGS SECTION

For external use only
Allergy alert:
If prone to allergic reaction from aspirin or salicylates, consult a doctor before use
Do not use
• on wounds or damaged skin
• with a heating pad
• if you are allergic to any ingredients of this product
When using this product
• use only as directed
• avoid contact with eyes or mucous membranes
• do not bandage tightly
• discontinue use at least 1 hour before bathing or showering
• do not use immediately after bathing or showering

Stop use and ask a doctor if
• skin reactions such as redness, itching, rash, excessive irritation, burning sensation, swelling or blistering occur
• conditions worsen or symptoms persist for more than 7 days
• symptoms clear up and occur again within a few days
If pregnant or breast-feeding, ask a health professional before use.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Heating Pain Relieving Patch — Inactive Ingredients
Arnica Extract, Aloe Vera Extract, Sunflower Extract, Rhubarb Extract, Myrrh Gum, Natural Rubber, Zinc Oxide, Adhesive
Cooling Pain Relieving Patch — Inactive Ingredients
Sunflower Extract, Rhubarb Extract, Myrrh Gum, Natural Rubber, Zinc Oxide, Adhesive

Indications & Usage

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints associated with:
• simple backache
• arthritis
• strains
• bruises
• sprains

OTC – Keep Out of Reach of Children

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.

OTC – Purpose

OTC - PURPOSE SECTION

Topical Analgesic

TERAPIA DE DIA Y NOCHE Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

TERAPIA DE DIA Y NOCHE 1TERAPIA DE DIA Y NOCHE 1

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87943-08587943-085-20
87943-01287943-012-01
87943-01687943-016-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

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 · 3 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
PARCHE CALIENTECAPSAICINA AND MENTOLDW SUPPORT LLC59f2708e-295a-ccb3-e063-6394a90ad3952026-08-26WarningsExact identifier
ndc (package): 87943-016-01
ndc (product): 87943-016
ndc11 (package): 87943001601
TERAPIA DE DIA Y NOCHEPAIN RELIEVING PATCHDW SUPPORT LLC59f44135-865b-9d7d-e063-6294a90a9dd92026-08-26WarningsExact identifier
ndc (package): 87943-012-01
ndc (package): 87943-016-01
ndc (package): 87943-085-20
ndc (product): 87943-085
ndc11 (package): 87943001601
ndc11 (package): 87943001201
ndc11 (package): 87943008520
spl id: 59f44135-865c-9d7d-e063-6294a90a9dd9
spl set id: 59f44135-865b-9d7d-e063-6294a90a9dd9
PARCHE FRIOMETHYL SALICYLATE, MENTHOL, AND CAMPHOR PATCHDW SUPPORT LLC5970a6f7-b273-9bb1-e063-6394a90afc792026-08-21WarningsExact identifier
ndc (package): 87943-012-01
ndc (product): 87943-012
ndc11 (package): 87943001201

Reported adverse events (FAERS/openFDA)#

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