ZIKS ARTHRITIS PAIN RELIEF

Product NDC: 63044-030
11-digit product format: 630440030
Labeler code: 63044
Product ID: 63044-030_04c250af-b544-4861-b5a8-94c5d9c070ac
Type: HUMAN OTC DRUG
Nonproprietary name: ZIKS ARTHRITIS PAIN RELIEF
Dosage form: CREAM
Route: TOPICAL
Labeler: Nnodum Pharmaceuticals
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 1999-11-10
Substance: METHYL SALICYLATE; MENTHOL; CAPSAICIN
Active strength: 6.79; .566; .014 mg/g; mg/g; mg/g
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 6 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2020-12-18 03:04 UTC · source 2020-12-17	excluded product	product		`e2bbac7714bc…`	`27bdfed8d636…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded package	package	63044-030-60	`e2bbac7714bc…`	`27bdfed8d636…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded product	product		`9bebd1f3094a…`	`5416666fcb17…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded package	package	63044-030-60	`9bebd1f3094a…`	`5416666fcb17…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded product	product		`110d247fa046…`	`a55b01930146…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded package	package	63044-030-60	`110d247fa046…`	`a55b01930146…`

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: ZIKS ARTHRITIS PAIN RELIEF
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
METHYL SALICYLATE	6.79 mg/g
MENTHOL	.566 mg/g
CAPSAICIN	.014 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
LAV5U5022Y	Internal UNII lookup
L7T10EIP3A	Internal UNII lookup
S07O44R1ZM	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
283224	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
5dd4fefc-b70a-4850-819c-1cca6f28aa97	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
473d070d-1c38-488e-b991-c4d1bf45aab8	Product name	1	20210201

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63044-030-60	2021-12-22	C162847	48780-1	956f9ecf-c4f5-621f-e053-dbdaa90a74ad	Arthritis Pain Relief Cream
63044-030-60	2019-10-21	C162847	48780-1	956f9ecf-c4f5-621f-e053-dbdaa90a74ad	Arthritis Pain Relief Cream

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63044-030-60	ZIKS ARTHRITIS PAIN RELIEF	56.6 g in 1 TUBE	CREAM	56.6		18

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
63044-030-60	GM - Gram	63044-030	b2ab0bbc-ca19-438f-a30a-db309312066c	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
CAPSAICIN	ACTIVE INGREDIENT	S07O44R1ZM	ZIKS ARTHRITIS PAIN RELIEF CREAM [NNODUM PHARMACEUTICALS]	5
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	ZIKS ARTHRITIS PAIN RELIEF CREAM [NNODUM PHARMACEUTICALS]	5
METHYL SALICYLATE	ACTIVE INGREDIENT	LAV5U5022Y	ZIKS ARTHRITIS PAIN RELIEF CREAM [NNODUM PHARMACEUTICALS]	5
CAPSAICIN	ACTIVE MOIETY	S07O44R1ZM	ZIKS ARTHRITIS PAIN RELIEF CREAM [NNODUM PHARMACEUTICALS]	5
MENTHOL	ACTIVE MOIETY	L7T10EIP3A	ZIKS ARTHRITIS PAIN RELIEF CREAM [NNODUM PHARMACEUTICALS]	5
METHYL SALICYLATE	ACTIVE MOIETY	LAV5U5022Y	ZIKS ARTHRITIS PAIN RELIEF CREAM [NNODUM PHARMACEUTICALS]	5
CETETH-20	INACTIVE INGREDIENT	I835H2IHHX	ZIKS ARTHRITIS PAIN RELIEF CREAM [NNODUM PHARMACEUTICALS]	5
CETYL ALCOHOL	INACTIVE INGREDIENT	936JST6JCN	ZIKS ARTHRITIS PAIN RELIEF CREAM [NNODUM PHARMACEUTICALS]	5
SORBITOL	INACTIVE INGREDIENT	506T60A25R	ZIKS ARTHRITIS PAIN RELIEF CREAM [NNODUM PHARMACEUTICALS]	5
UREA	INACTIVE INGREDIENT	8W8T17847W	ZIKS ARTHRITIS PAIN RELIEF CREAM [NNODUM PHARMACEUTICALS]	5
WATER	INACTIVE INGREDIENT	059QF0KO0R	ZIKS ARTHRITIS PAIN RELIEF CREAM [NNODUM PHARMACEUTICALS]	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63044-030	ZIKS ARTHRITIS PAIN RELIEF CREAM [NNODUM PHARMACEUTICALS]	17	Current NDC, Legacy NDC, 1 package rows	20241230_5dd4fefc-b70a-4850-819c-1cca6f28aa97.zip

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 136 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Leader Burn Relief	LIDOCAINE	Cardinal Health	f4e8e3b7-fd84-bdbc-e053-2a95a90aeab2	2024-02-06	Warnings	Exact identifier application number: M017
Pain Relieving Petro Carbo	PHENOL	J.R. Watkins, LLC.	050cf17d-3be7-45b9-8524-ad82af309a0e	2024-02-06	Warnings	Exact identifier application number: M017
White Cream	CAMPHOR (NATURAL) AND TURPENTINE OIL	J.R. Watkins, LLC.	e4de0734-59d5-478c-86ea-66fc2ba003e7	2024-02-05	Warnings	Exact identifier application number: M017
Pain Relieving Roll-On	MENTHOL, UNSPECIFIED FORM	Safetec of America, Inc.	80118260-9c88-402d-9a90-ecfe62b4b54f	2024-02-05	Warnings	Exact identifier application number: M017
Pain Relieving	MENTHOL, UNSPECIFIED FORM	Safetec of America, Inc.	df512ce6-ce1b-434d-9571-fb2e1d76e1d0	2024-02-05	Warnings	Exact identifier application number: M017
Pain Relieving	MENTHOL	Safetec of America, Inc.	52ebf64d-095f-467e-bf51-dd8d33b58c7d	2024-02-05	Warnings	Exact identifier application number: M017
Itch Relief	DIPHENHYDRAMINE HYDROCHLORIDE	Safetec of America, Inc.	4f4c801b-d894-4fa3-b024-6ca41a5f2a95	2024-02-04	Warnings	Exact identifier application number: M017
Analgesic	MENTHOL	Safetec of America, Inc.	79e3b0e7-4ba5-4b9d-a980-5b6f18dba802	2024-02-04	Warnings	Exact identifier application number: M017
HAV EZ Penetrating Pain Relief	MENTHOL	PALM ORTHOPEDICS & INTERVENTIONAL PAIN LLC	70006efc-9cc8-4490-b28c-fcb23b1737c4	2024-02-01	Warnings	Exact identifier application number: M017
Rugby Capsaicin External Analgesic	CAPSAICIN	Proficient Rx LP	7c733a30-5002-49e7-a6bd-7737a1d2461e	2024-02-01	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE	Proficient Rx LP	ccb62898-b614-45b9-95ea-23e5e31893a8	2024-02-01	Warnings	Exact identifier application number: M017
Hydrocortisone with Aloe	HYDROCORTISONE	Proficient Rx LP	0b26d92f-9d0e-46d4-a8bc-75d6da5f6199	2024-02-01	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE	Proficient Rx LP	c57d5f8e-5934-4cbb-999a-cdd55e5b105f	2024-02-01	Warnings	Exact identifier application number: M017
hydrocortisone	HYDROCORTISONE	Proficient Rx LP	47e9fe84-bd0c-40ea-85de-e950bcacc557	2024-02-01	Warnings	Exact identifier application number: M017
Joint and Muscle Pain	MENTHOL	Shaklee Corporation	3943824f-1f4f-4d6f-bd73-0b1be02162a5	2024-01-30	Warnings	Exact identifier application number: M017
Mirakel Pain Relief Roll-On	LIDOCAINE HCL	Sanvio, Inc.	102f3618-13ad-37e3-e063-6294a90a8086	2024-01-30	Warnings	Exact identifier application number: M017
Blistex Lip Medex	PETROLATUM, MENTHOL, UNSPECIFIED FORM, CAMPHOR (SYNTHETIC), AND PHENOL	Blistex Inc.	8ad39005-9419-4f1a-a1ae-2f76d212455e	2024-01-26	Warnings	Exact identifier application number: M017
Point Relief Cold Spot Pain Relieving	MENTHOL	Fabrication Enterprises	ad5d6f04-15e6-4548-95c2-32271c186bc1	2024-01-25	Warnings	Exact identifier application number: M017
MIND BODY MATRIX PAIN RELIEF	MENTHOL	Functional Energetic, Inc.	3667dd0d-942e-4101-ba98-cb013ae77cf5	2024-01-25	Warnings	Exact identifier application number: M017
SUPER WHITE STUFF Pain Relief	MENTHOL	BLUE SPRING WELLNESS	e6d27df5-118c-4c6d-86e8-7b4401a39c76	2024-01-23	Warnings	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
LAV5U5022Y	METHYL SALICYLATE	119-36-8	METHYL SALICYLATE
S07O44R1ZM	CAPSAICIN	404-86-4	CAPSAICIN

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
283224	capsaicin 0.025 % / menthol 1 % / methyl salicylate 12 % Topical Cream	PSN	5dd4fefc-b70a-4850-819c-1cca6f28aa97	18
283224	capsaicin 0.25 MG/ML / menthol 10 MG/ML / methyl salicylate 120 MG/ML Topical Cream	SCD	5dd4fefc-b70a-4850-819c-1cca6f28aa97	18
283224	capsaicin 0.025 % / menthol 1 % / methyl salicylate 12 % Topical Cream	SY	5dd4fefc-b70a-4850-819c-1cca6f28aa97	18

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63044-030-60	63044003060	56.6 g in 1 TUBE (63044-030-60)	56.6 g	1999-11-10	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Arthritis Pain Relief Cream	Nnodum Pharmaceuticals \| Contract Pharmacal Corporation	2025-12-29	HUMAN OTC DRUG LABEL	18