ActivOn Ultra Strength Arthritis

Manufacturer
Family First Pharmaceuticals, Inc. | RNA Pharma, LLC
Effective date
2017-02-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:48:52

Label at a glance#

ProductActivOn Ultra Strength Arthritis
Active ingredientMenthol, Unspecified Form
Label structure11 sections

Indications and uses

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

Dosage and administration

adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily. children under 12 years of age: ask a doctor

Storage and handling

Keep away from heat. Store between 15° and 30° C (59° and 86° F).

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 5.138%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

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.

Do not use

OTC - DO NOT USE SECTION

  • otherwise than as directed
  • if you are allergic to any ingredient in this product
  • on a child under 12 years of age with arthritis-like conditions
  • with a heating pad

When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes, wounds, mucous membranes, broken or irritated skin
  • do not share this product with anyone
  • do not bandage tightly

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

  • condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days
  • skin redness or excessive irritation of the skin develops

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children. If swallowed, get mediacal help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily.
  • children under 12 years of age: ask a doctor

Other information

STORAGE AND HANDLING SECTION

Keep away from heat. Store between 15° and 30° C (59° and 86° F).

Inactive Ingredients

INACTIVE INGREDIENT SECTION

diazolidinyl urea, ethyl alcohol, iodopropynyl butylcarbamate, menthyl lactate, propylene glycol, sodium stearate, steareth-21, tetrasodium EDTA, triethanolamine, water

Questions ?

OTC - QUESTIONS SECTION

call 1-800-379-8870, Weekdays 9AM to 5PM EST

SPL UNCLASSIFIED SECTION

Dist. by Family First Pharmaceuticals, Inc., Reno, NV 89502

PRINCIPAL DISPLAY PANEL - 57 g Canister Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NEW STRONGEST

ACTIVON® ARTHRITIS

ACTIVON®
Topical Analgesic

ULTRA
STRENGTH
ARTHRITIS

Powerful Pain Relief
for Arthritis &
Joint & Muscle Pain

No-Mess

NDC 51068-507-01
NET WT 2 OZ (57 g)

PRINCIPAL DISPLAY PANEL - 57 g Canister Carton
PRINCIPAL DISPLAY PANEL - 57 g Canister Carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1148640ActivOn Ultra Strength Joint & Muscle 5.138 % Topical CreamPSN1
1148638menthol 5.14 % Topical CreamPSN1
1148640menthol 51.4 MG/ML Topical Cream [ActivOn Joint & Muscle]SBD1
1148638menthol 51.4 MG/ML Topical CreamSCD1
1148640ActivOn Joint & Muscle 51.4 MG/ML Topical CreamSY1
1148640ActivOn Ultra Strength Joint & Muscle 5.138 % Topical CreamSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51068-507-012020-01-31C16284748780-19d75b9d0-ade3-f424-e053-dadaa90a57ceActivOn ® Ultra Strength Arthritis

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51068-507-01ActivOn Ultra Strength Arthritis1 in 1 CARTONSTICK11
51068-507-01ActivOn Ultra Strength Arthritis57 g in 1 CANISTERSTICK571

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51068-507ACTIVON ULTRA STRENGTH ARTHRITIS (MENTHOL, UNSPECIFIED FORM) STICK [FAMILY FIRST PHARMACEUTICALS, INC.]1Legacy NDC, 2 package rows20170222_09d6b5a1-9223-4b60-b92d-7883a434a13e.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51068-50751068-507-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
315fd1be-ae83-460e-96ac-e8117ded1dd709d6b5a1-9223-4b60-b92d-7883a434a13e2017-02-21WarningsExact identifier
spl id: 315fd1be-ae83-460e-96ac-e8117ded1dd7
spl set id: 09d6b5a1-9223-4b60-b92d-7883a434a13e

Reported adverse events (FAERS/openFDA)#

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