Home NDC 63044-030 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.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# 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 Socrata Ingredients# 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 109 of 153 · 3,057 matching rows.
DailyMed RxNorm Mappings# 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