Good Neighbor Medicated Relief Patches

Manufacturer
Amerisource Bergen | Foshan Aqua Gel Biotech Co.,Ltd.
Effective date
2026-08-20
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
daily-update
Hydrated at
2026-08-25 01:03:28

Label at a glance#

ProductPain Relief Patches
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE
Label structure9 sections

Indications and uses

For temporary relief of minor aches and pains of muscles and joints associated with arthritis, simple backache, strains, sprains, and bruises.

Dosage and administration

Adults and children 12 years of age and over: Clean and dry affected area. Remove patch from film, apply to affected area not more than 3 to 4 times daily. Remove patch from the skin after at most, 8-hour application. Children under 12 years of age: consult physician. Hydrogenated Poly, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Petroleum, Styrene / Isoprene Copolymer For temporary relief of minor ach...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients Purpose

Camphor 3.1% ......................Topical Analgesic

Menthol 6.0% .......................Topical Analgesic

Methyl Salicylate 10.0% .......Topical Analgesic

For External Use Only

WARNINGS SECTION

Allergy alert: If prone to allergic reaction from aspirin or salicylates, consult a doctor before use

Do not use:

OTC - DO NOT USE SECTION

  • On wounds or damaged skin
  • With a heating pad
  • If you are allergic to any ingredients of this product

When using this product

OTC - WHEN USING SECTION

  • Use only as directed
  • Avoid contact with eyes, mucous membranes or rashes
  • Do not bandage tightly
  • Do not use at the same time as other topical analgesics
  • Dispose of used patch in manner that keeps product away from children and pets. Used patches still contain the drug product that can produce serious adverse effects if a child or pet chews or ingests this patch.

Stop use and consult a doctor

OTC - STOP USE SECTION

  • If rash, itching or excessive skin irritation develops
  • If condition worsens
  • if symptoms last more than 7 days or clear up and occur again with a few days

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away

Uses

OTC - PURPOSE SECTION

For temporary relief of minor aches and pains of muscles and joints associated with arthritis, simple backache, strains, sprains, and bruises.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and over: Clean and dry affected area. Remove patch from film, apply to affected area not more than 3 to 4 times daily. Remove patch from the skin after at most, 8-hour application.

Children under 12 years of age: consult physician.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Hydrogenated Poly, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Petroleum, Styrene / Isoprene Copolymer

Indication and Usage

INDICATIONS & USAGE SECTION

For temporary relief of minor aches and pains.

Pain Relief Patch Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Box of 20
NDC:46122-392-60
Box of 20Box of 20

Box of 40
NDC:46122-392-58
Box of 40Box of 40

Box of 60
NDC:46122-392-72
Box of 60Box of 60

Other Information: Store in clean, dry place outside of direct sunlight. Protect from excessive moisture.

DIST. BY
AmerisourceBergen
1300 Morris Drive
Chesterbrook, PA 19087
www.mygnp.com

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
46122-392-58EA - Each46122-39273a91acd-f7c8-4ba3-88a2-0458043bfd4712020-05-08
46122-392-60EA - Each46122-392848ee7f5-1f8a-4545-b324-da57955327e512022-06-06
46122-392-72EA - Each46122-39217ab1da1-a68f-426f-ba31-fd1b5fa36c5312020-05-08

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
46122-39246122-392-60, 46122-392-58, 46122-392-72

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
62025-12-22full-release2026-06-01 01:28:09

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
Pain Relief PatchesCAMPHOR, MENTHOL, METHYL SALICYLATEAmerisource Bergen5fb5e5ce-b268-4444-8b63-ea7ea6abf2692026-08-20WarningsExact identifier
ndc (package): 46122-392-58
ndc (package): 46122-392-72
ndc (package): 46122-392-60
ndc (product): 46122-392
ndc11 (package): 46122039260
ndc11 (package): 46122039258
ndc11 (package): 46122039272
spl id: 598412f5-3837-bbf9-e063-6394a90a6784
spl set id: 5fb5e5ce-b268-4444-8b63-ea7ea6abf269

Reported adverse events (FAERS/openFDA)#

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