Absorbine Jr. Pain Relieving Knee Patch

Manufacturer
Clarion Brands, LLC
Effective date
2025-12-28
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:28:57

Label at a glance#

ProductAbsorbine Jr. Pain Relieving Knee Patch
Active ingredientMENTHOL
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Menthol 7.5%

OTC - PURPOSE SECTION

Topical analgesic

INDICATIONS & USAGE SECTION

For temporary relief of minor aches and pains of muscles and joints associated with:

  • simple backache
  • arthritis
  • sprains
  • strains
  • bruises

WARNINGS SECTION

For external use only. 

Do not use

  • on wounds or damaged skin
  • with a heating pad

Ask a doctor before use if you have

  • redness over affected area

When using this product

  • avoid contact with eyes and mucous membranes
  • do not bandage tightly

Stop use and ask a doctor if

  • condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days
  • excessive skin irritation occurs

INDICATIONS & USAGE SECTION

  • adults and children 12 years of age and older apply to the affected area no more than 3 to 4 times daily
  • open pouch & remove patch
  • peel off protective film and apply sticky side to affected area
  • children under 12 years of age consult a doctor

INACTIVE INGREDIENT SECTION

  • glyceryl hydrogenated rosinate
  • hydrated silica
  • mineral oil
  • PEG-400
  • polyisobutylene
  • styrene/isoprene copolymer

OTC - QUESTIONS SECTION

call 1-844-822-7672

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 - ASK DOCTOR SECTION

Ask a doctor before use if you have

  • redness over affected area

DOSAGE & ADMINISTRATION SECTION

Menthol 7.5%

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Lasts up to 8 Hours!

Absorbine jr.®
QUALITY RELIEF SINCE 1903

DEEP PENETRATING & FAST ACTING PAIN RELIEF

PAIN RELIEVING KNEE PATCH


7.5% Menthol 

Relieves Knee, Elbow & Joint Pain

• Penetrates Deep & Starts to Work Instantly
• Sweat Proof Technology to Stay in Place Securely
• Customizable for Any Size Knee

Medicated Patch
1 Knee 8 × 6 in (20 × 15 cm)

POWERFUL TARGETED RELIEF


Absorbine jr.®
QUALITY RELIEF SINCE 1903

THE ORIGINAL PAIN RELIEF

The Absorbine Jr. Knee Patch formula is specifically developed

to provide relief from regular and activity induced knee & joint

aches and pains.


Distributed by:
Absorbine Jr. LLC
811 Broad Street, Suite 600 
Chattanooga, TN 37402
1000381 @2025
www.absorbinejr.com

Made in China

ABS Jr Knee Patch labelABS Jr Knee Patch label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69693-423-01Absorbine Jr. Pain Relieving Knee Patch1 h in 1 POUCHPATCH13

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69693-42369693-423-01

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

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
Absorbine Jr. Pain Relieving Knee PatchABSORBINE JR. PAIN RELIEVING KNEE PATCHClarion Brands, LLC22f71254-e521-2d82-e063-6394a90a12d82025-12-28WarningsExact identifier
ndc (package): 69693-423-01
ndc (product): 69693-423
ndc11 (package): 69693042301
spl id: 470ea034-95a2-dfe4-e063-6394a90aa63e
spl set id: 22f71254-e521-2d82-e063-6394a90a12d8

Reported adverse events (FAERS/openFDA)#

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