Arthritis Pain Relief Cream

Manufacturer
Nnodum Pharmaceuticals | Contract Pharmacal Corporation
Effective date
2025-12-29
Label type
HUMAN OTC DRUG LABEL
Version
18
Source
full-release
Hydrated at
2026-06-01 01:29:14

Label at a glance#

ProductZIKS ARTHRITIS PAIN RELIEF
Active ingredientMETHYL SALICYLATE, MENTHOL, CAPSAICIN
Label structure8 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: consult a physician. A passing burning sensation may occur upon application, but generally disappears in several days. Application schedules of less than 3 to 4 times a day may not provide optimum pain relief ant the burning sensation may persist. WASH HANDS WITH SOAP AND WATER AFTE...

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - PURPOSE SECTION

Methyl Salicylate 12%, Menthol 1% and Capsaicin 0.025%

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Methyl Salicylate 12%, Menthol 1% and Capsaicin 0.025%

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Cetyl Alcohol, Ceteth-2, Sorbitol Solution, Imidazolidinyl Urea and Purified Water.

INDICATIONS:

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pain of muscles and joints associated with arthritis, simple backache, strains and sprains. *Products containing purified capsaicin are most recommended by doctors and pharmacists.

DIRECTIONS:

DESCRIPTION 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: consult a physician. A passing burning sensation may occur upon application, but generally disappears in several days. Application schedules of less than 3 to 4 times a day may not provide optimum pain relief ant the burning sensation may persist. WASH HANDS WITH SOAP AND WATER AFTER APPLYING UNLESS TREATING HANDS.

WARNING:

WARNINGS SECTION

For external use only. Avoid contact with eyes and mucus membranes. If conditions worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician. Do not apply to wounds, damage or broken (open), irritated skin or excessive irritation develops.

Do not bandage tightly. Do not use with heating pad. As with any drug, if you are pregnant or nursing a baby, seek the advice of a health professional before using this product. Keep this and all drugs out of the reach of children. In case of accidental ingestion, seek professional assistance or contact a poison control center immediately.

Storage

Store at room temperature 15-30 degrees C (59-86 degrees F). Lot number and expiration date: See tube seal area or end flap.

How Supplied:

HOW SUPPLIED SECTION

Ziks cream is supplied in a 2 oz. tube.

Distributed by: ZIKS Healthcare Products, Cincinnati, OH 45229

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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8faec0ee-figure-01

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
283224capsaicin 0.025 % / menthol 1 % / methyl salicylate 12 % Topical CreamPSN18
283224capsaicin 0.25 MG/ML / menthol 10 MG/ML / methyl salicylate 120 MG/ML Topical CreamSCD18
283224capsaicin 0.025 % / menthol 1 % / methyl salicylate 12 % Topical CreamSY18

DailyMed Product Concepts#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63044-030-602021-12-22C16284748780-1956f9ecf-c4f5-621f-e053-dbdaa90a74adArthritis Pain Relief Cream
63044-030-602019-10-21C16284748780-1956f9ecf-c4f5-621f-e053-dbdaa90a74adArthritis Pain Relief Cream

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63044-030-60ZIKS ARTHRITIS PAIN RELIEF56.6 g in 1 TUBECREAM56.618

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63044-030-60GM - Gram63044-030b2ab0bbc-ca19-438f-a30a-db309312066c12012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CAPSAICINACTIVE INGREDIENTS07O44R1ZM5
MENTHOLACTIVE INGREDIENTL7T10EIP3A5
METHYL SALICYLATEACTIVE INGREDIENTLAV5U5022Y5
CAPSAICINACTIVE MOIETYS07O44R1ZM5
MENTHOLACTIVE MOIETYL7T10EIP3A5
METHYL SALICYLATEACTIVE MOIETYLAV5U5022Y5
CETETH-20INACTIVE INGREDIENTI835H2IHHX5
CETYL ALCOHOLINACTIVE INGREDIENT936JST6JCN5
SORBITOLINACTIVE INGREDIENT506T60A25R5
UREAINACTIVE INGREDIENT8W8T17847W5
WATERINACTIVE INGREDIENT059QF0KO0R5

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
63044-03063044-030-60

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 10 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
CETETH-20CETETH-20I835H2IHHXCREAM / TOPICAL429 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
UREAUREA8W8T17847WSYSTEM / TOPICAL840 mgExact identifier — unii+route
4 equally ranked IID candidates
CETETH-20CETETH-20I835H2IHHXCREAM / TOPICAL429 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
UREAUREA8W8T17847WSYSTEM / TOPICAL840 mgExact identifier — unii+route
4 equally ranked IID candidates
UREAUREA8W8T17847WCREAM / VAGINAL0.64 %w/wExact identifier — unii+dosage form
4 equally ranked IID candidates
SORBITOLSORBITOL506T60A25RCREAM / TOPICAL36.8 %w/wExact identifier — unii+route+dosage form
2 equally ranked IID candidates
CETYL ALCOHOLCETYL ALCOHOL936JST6JCNCREAM / TOPICAL1280 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
SORBITOLSORBITOL506T60A25RCREAM / TOPICAL36.8 %w/wExact identifier — unii+route+dosage form
2 equally ranked IID candidates
UREAUREA8W8T17847WCREAM / VAGINAL0.64 %w/wExact identifier — unii+dosage form
4 equally ranked IID candidates
CETYL ALCOHOLCETYL ALCOHOL936JST6JCNCREAM / TOPICAL1280 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates

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
ZIKS ARTHRITIS PAIN RELIEFZIKS ARTHRITIS PAIN RELIEFNnodum Pharmaceuticals5dd4fefc-b70a-4850-819c-1cca6f28aa972025-12-29WarningsExact identifier
ndc (package): 63044-030-60
ndc (product): 63044-030
ndc11 (package): 63044003060
spl id: 04c250af-b544-4861-b5a8-94c5d9c070ac
spl set id: 5dd4fefc-b70a-4850-819c-1cca6f28aa97

Reported adverse events (FAERS/openFDA)#

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