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OTC products · Product label record

Terapia De Dia Y Noche drug information

PAIN RELIEVING PATCH
DW SUPPORT LLC · TOPICAL

Product NDC: 87943-085

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic namePAIN RELIEVING PATCH
Labeler / manufacturerDW SUPPORT LLC
RouteTOPICAL
Drug classDrug class not supplied in source label
Product NDC87943-085
Label effective date2026-08-26

Official product label reference

Terapia De Dia Y Noche — DW SUPPORT LLC

This page contains 6 source sections for PAIN RELIEVING PATCH, topical route. Label set 59f44135-865b-9d7d-e063-6294a90a9dd9, version 1.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

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

Purpose

OTC – Purpose Topical Analgesic
Dosage and administration — label text
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 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 ingredient
Inactive Ingredients 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
Child safety
OTC – Keep Out of Reach of Children Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Official sources and product identifiers

RxNorm identifiers: 1793147, 2750061

Package NDC codes

87943-085-20, 87943-012-01, 87943-016-01

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.