QNTAMAX Muscle & Joint Pain Relieving Ointment

Manufacturer
Qntamax LLC
Effective date
2026-01-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:31:45

Label at a glance#

ProductQNTAMAX Muscle and Joint Pain Relieving
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL
Label structure7 sections

Dosage and administration

Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily.  Children under 2 years of age: do not use, consult a doctor.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor 4%
Menthol 5%

Purpose

OTC - PURPOSE SECTION

Pain Relieving

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

  • avoid contact with the eyes
  • do not apply to wounds or damaged skin
  • do not bandage tightly

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens
  • symptoms last more than 7 days or clear up and occur again within 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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. 
  • Children under 2 years of age: do not use, consult a doctor.

Other information

SPL UNCLASSIFIED SECTION

  • Store in a cool, dry place.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Arnica Extract ( Arnica Montana), Avocado Oil ( Persea gratissima), Beeswax ( Cera alba), Caprylic/Capric Triglyceride, Capsaicin, Ginger Root Oil ( Zingiber officinale), Grapeseed Seed Oil ( Vitis vinifera), Lavender Oil ( Lavandula angustifolia), Meadowfoam Seed Oil ( Limnanthes alba), Peppermint Oil ( Mentha piperita), Turmeric Root Extract ( Curcuma longa), Tocopherol.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer PackageOuter PackageInner PackageInner Package

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2727392camphor 4 % / menthol 5 % Topical OintmentPSN2
2727392camphor 0.04 MG/MG / menthol 0.05 MG/MG Topical OintmentSCD2
2727392camphor 4 % / menthol 5 % Topical OintmentSY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
473d070d-1c38-488e-b991-c4d1bf45aab8Product name120210201

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85892-000-00QNTAMAX Muscle and Joint Pain Relieving37 g in 1 JAROINTMENT372
85892-000-00QNTAMAX Muscle and Joint Pain Relieving1 in 1 CARTONOINTMENT12

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85892-00085892-000-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-09-18monthly-update2026-06-03 17:39:48

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
QNTAMAX Muscle and Joint Pain RelievingCAMPHOR (SYNTHETIC), MENTHOLQntamax LLC6622b94c-824e-4e84-a8d8-b60bb0b866e22026-01-06WarningsExact identifier
ndc (package): 85892-000-00
ndc (product): 85892-000
ndc11 (package): 85892000000
spl id: 47b8ba87-db0b-3b9d-e063-6294a90a49b4
spl set id: 6622b94c-824e-4e84-a8d8-b60bb0b866e2

Reported adverse events (FAERS/openFDA)#

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