Home NDC 69842-301 CVS Arthritis Pain Relief
Product NDC 69842-301
11-digit product format 698420301
Labeler code 69842
Product ID 69842-301_6242f79a-934b-4232-b66b-d41db041e6b8
Type HUMAN OTC DRUG
Nonproprietary name Arthritis Pain Relief
Dosage form CREAM
Route TOPICAL
Labeler CVS Health
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2016-05-30
Substance HISTAMINE DIHYDROCHLORIDE
Active strength .025 g/100g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes 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 CVS Arthritis Pain Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HISTAMINE DIHYDROCHLORIDE .025 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3POA0Q644U Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1091387 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69842-301-60 CVS Arthritis Pain Relief 113 g in 1 JAR CREAM 113 2 69842-301-60 CVS Arthritis Pain Relief 1 in 1 CARTON CREAM 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69842-301 CVS ARTHRITIS PAIN RELIEF (ARTHRITIS PAIN RELIEF) CREAM [CVS HEALTH] 2 Current NDC, Legacy NDC, 2 package rows 20241113_575dd514-fd99-4e44-8fc8-52938f9abc26.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 90 of 152 · 3,029 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Curist 5% Lidocaine LIDOCAINE 5% Little Pharma, Inc. f20241a2-c5b1-f124-e053-2995a90a891b 2025-06-16 Warnings Exact identifier application number: M017 Toast Screamin Menthol MENTHOL IDEAZ, LLC 37b48b1a-ef3d-afdc-e063-6294a90a6610 2025-06-16 Warnings Exact identifier application number: M017 Toast Freezin Cold MENTHOL, METHYL SALICYLATE IDEAZ, LLC 37b4d363-0099-8cd3-e063-6394a90a18d6 2025-06-16 Warnings Exact identifier application number: M017 Earths Care Anti-Itch CAMPHOR (NATURAL) AND MENTHOL, UNSPECIFIED FORM DLC Laboratories, Inc. ba65f58a-d590-498a-b8e7-a3d78935d880 2025-06-13 Warnings Exact identifier application number: M017 Lidocaine LIDOCAINE Stratus Pharmaceuticals Inc 5eb6574c-2066-4390-befc-8e5d2dd6ede2 2025-06-12 Warnings Exact identifier application number: M017 CHINESE RED TIGER LIDOCAINE PATCHES 4% LIDOCAINE, 1%MENTHOL Guangzhou Zhupuyou E-commerce Co., Ltd 36b9a7a2-5832-4ce5-e063-6294a90aed12 2025-06-12 Warnings Exact identifier application number: M017 PRO COLD HOT Pain Relief Gel Roll-On (Plantar Fasciitis) MENTHOL Guangzhou Zhupuyou E-commerce Co., Ltd 375bc794-3289-e610-e063-6294a90a4f9b 2025-06-12 Warnings Exact identifier application number: M017 Methyl Salicylate 10% Pain Relieving METHYL SALICYLATE PureTek Corporation 376493eb-5142-db6d-e063-6294a90a1e73 2025-06-12 Warnings Exact identifier application number: M017 Free and Pure Cold Therapy Pain Relief MENTHOL Walgreen Co. 22cbbffc-f876-411e-e063-6394a90a1b38 2025-06-12 Warnings Exact identifier application number: M017 Methylten 25% Pain Relieving METHYL SALICYLATE PureTek Corporation 3767b97e-ab0c-ac26-e063-6394a90a00cf 2025-06-12 Warnings Exact identifier application number: M017 SPF 50 Mineral Sunscreen ZINC OXIDE Inspec Solutions, LLC 36af9a0a-536b-ee1a-e063-6394a90aace4 2025-06-11 Warnings Exact identifier application number: M017 PLANTAR FASCIITIS Relief Gel Roll-On MENTHOL Guangzhou Zhupuyou E-commerce Co., Ltd 37570149-dae1-a4f2-e063-6294a90a3245 2025-06-11 Warnings Exact identifier application number: M017 Diabecin CS Cream MENTHOL, CAPSAICIN Puretek Corporation 33ef2233-7a66-ee65-e063-6294a90ac55a 2025-06-10 Warnings Exact identifier application number: M017 KINKAN COOL DIPHENHYDRAMINE HYDROCHLORIDE, MENTHOL KINKANDO CO., LTD . 82011efe-825c-4102-b6f1-59eff4c8040a 2025-06-10 Warnings Exact identifier application number: M017 MQUPIN Knee Patch KNEE PATCH Zhengzhou Miaoqi Medical Technology Co., Ltd. 37438a70-dab7-ecb5-e063-6394a90afefb 2025-06-10 Warnings Exact identifier application number: M017 ORTHOGEL Menthol 3.5% Roll On MENTHOL LiquidCapsule Manufacturing LLC 99424327-67e9-43b5-a117-94c9643413c1 2025-06-07 Warnings Exact identifier application number: M017 Lightning Pain Relief MENTHOL Ebanel Laboratories, Inc 36edbc3f-501c-c1ea-e063-6394a90af6af 2025-06-06 Warnings Exact identifier application number: M017 FREEZE IT Menthol Roll On MENTHOL LiquidCapsule Manufacturing LLC 33094afe-db9d-4b92-8047-6dd611484fc9 2025-06-05 Warnings Exact identifier application number: M017 Band Aid Antiseptic Cleansing BENZALKONIUM CHLORIDE, PRAMOXINE HCL Kenvue Brands LLC d55e6b09-0587-61a9-e053-2995a90afaf5 2025-06-05 Warnings Exact identifier application number: M017 FREEZE IT Menthol MENTHOL LiquidCapsule Manufacturing LLC de8d8007-5718-4fb4-a8c6-4650d2ca9c8f 2025-06-05 Warnings Exact identifier application number: M017
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 69842-301-60 69842030160 1 JAR in 1 CARTON (69842-301-60) / 113 g in 1 JAR 1 jar 2016-05-30 0000-00-00 No No Current