Home NDC 52241-100 Katinko Pain And Itch Relieving
Product NDC 52241-100
11-digit product format 522410100
Labeler code 52241
Product ID 52241-100_0c0d4eac-3530-250d-e063-6294a90aad14
Type HUMAN OTC DRUG
Nonproprietary name CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE
Dosage form OINTMENT
Route TOPICAL
Labeler Greenstone Pharmaceutical Inc.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2010-05-24
Substance CAMPHOR (SYNTHETIC); MENTHOL; METHYL SALICYLATE
Active strength 11; 7.6; 13 g/100g; g/100g; g/100g
NDC exclude flag No
Listing certified through 2027-12-31
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 Katinko Pain And Itch Relieving
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAMPHOR (SYNTHETIC) 11 g/100g MENTHOL 7.6 g/100g METHYL SALICYLATE 13 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5TJD82A1ET Internal UNII lookup L7T10EIP3A Internal UNII lookup LAV5U5022Y Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1542816 Internal RxNorm lookup 1542818 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 52241-100-03 Katinko Pain And Itch Relieving 1 in 1 CARTON OINTMENT 1 8 52241-100-03 Katinko Pain And Itch Relieving 3 g in 1 JAR OINTMENT 3 8 52241-100-10 Katinko Pain And Itch Relieving 1 in 1 CARTON OINTMENT 1 8 52241-100-10 Katinko Pain And Itch Relieving 10 g in 1 JAR OINTMENT 10 8 52241-100-30 Katinko Pain And Itch Relieving 30 g in 1 BOTTLE OINTMENT 30 8 52241-100-30 Katinko Pain And Itch Relieving 1 in 1 CARTON OINTMENT 1 8
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded CAMPHOR (SYNTHETIC) ACTIVE INGREDIENT 5TJD82A1ET KATINKO PAIN AND ITCH RELIEVING (CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE) OINTMENT [GREENSTONE PHARMACEUTICAL H.K. INC. ] 2 MENTHOL ACTIVE INGREDIENT L7T10EIP3A KATINKO PAIN AND ITCH RELIEVING (CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE) OINTMENT [GREENSTONE PHARMACEUTICAL H.K. INC. ] 2 METHYL SALICYLATE ACTIVE INGREDIENT LAV5U5022Y KATINKO PAIN AND ITCH RELIEVING (CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE) OINTMENT [GREENSTONE PHARMACEUTICAL H.K. INC. ] 2 CAMPHOR (SYNTHETIC) ACTIVE MOIETY 5TJD82A1ET KATINKO PAIN AND ITCH RELIEVING (CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE) OINTMENT [GREENSTONE PHARMACEUTICAL H.K. INC. ] 2 MENTHOL ACTIVE MOIETY L7T10EIP3A KATINKO PAIN AND ITCH RELIEVING (CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE) OINTMENT [GREENSTONE PHARMACEUTICAL H.K. INC. ] 2 SALICYLIC ACID ACTIVE MOIETY O414PZ4LPZ KATINKO PAIN AND ITCH RELIEVING (CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE) OINTMENT [GREENSTONE PHARMACEUTICAL H.K. INC. ] 2 PARAFFIN INACTIVE INGREDIENT I9O0E3H2ZE KATINKO PAIN AND ITCH RELIEVING (CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE) OINTMENT [GREENSTONE PHARMACEUTICAL H.K. INC. ] 2 PETROLATUM INACTIVE INGREDIENT 4T6H12BN9U KATINKO PAIN AND ITCH RELIEVING (CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE) OINTMENT [GREENSTONE PHARMACEUTICAL H.K. INC. ] 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 52241-100 KATINKO PAIN AND ITCH RELIEVING (CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE) OINTMENT [GREENSTONE PHARMACEUTICAL INC.] 8 Current NDC, Legacy NDC, 6 package rows 20231210_fe907fa4-4a01-4974-b71f-9cd980b4eaa2.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 72 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Coralite Muscle and Joint Pain Relief CAPSACIN United Exchange Corp. ba9a3d72-db7a-4dd0-9220-f43c9ed87114 2025-10-21 Warnings Exact identifier application number: M017 Coralite Extra Strength Pain Relief Sleeve Wrist MENTHOL United Exchange Corp. ae314478-b8ab-4e90-bd0a-7a882d5c1b2e 2025-10-21 Warnings Exact identifier application number: M017 Coralite Cold and Hot MENTHOL United Exchange Corp. 85bd7658-e951-7daf-e053-2a91aa0a9f54 2025-10-21 Warnings Exact identifier application number: M017 Family Care Maximum Strength Medicated Anti Itch MENTHOL United Exchange Corp. 430b5753-3087-4cb1-bf54-0eedc3f4b1d5 2025-10-21 Warnings Exact identifier application number: M017 Family Care Anti-Itch HYDROCORTISONE United Exchange Corp. 8e4d46d8-7084-0666-e053-2995a90ad520 2025-10-21 Warnings Exact identifier application number: M017 Coralite Pain Relief CAMPHOR, MENTHOL, METHYL SALICYLATE United Exchange Corp. 69aec845-3d4c-d226-e053-2991aa0afd12 2025-10-21 Warnings Exact identifier application number: M017 WHITE FLOWER ANALGESIC BALM CAMPHOR, MENTHOL AND METHYL SALICYLATE HOE HIN PAK FAH YEOW MANUFACTORY LTD f3e3b8b5-b12b-49ac-9318-b0c358b136e9 2025-10-21 Warnings Exact identifier application number: M017 Mountain Ice Sports Recovery MENTHOL Mountainside Medical Equipment, Inc. 98638529-3c17-436e-901f-c8aea52bdab6 2025-10-20 Warnings Exact identifier application number: M017 Lip Clear Lysine Plus MENTHOL, UNSPECIFIED FORM Quantum, Inc. 21a5b4fb-baed-4766-9820-5c6051c14720 2025-10-20 Warnings Exact identifier application number: M017 Buzz Away Sting Soothe MENTHOL Quantum, Inc. 419e34ea-17b2-ec32-e063-6394a90a603d 2025-10-20 Warnings Exact identifier application number: M017 Family Care Anti-Itch HYDROCORTISONE United Exchange Corp. deb09e89-9794-89a7-e053-2a95a90abdf8 2025-10-20 Warnings Exact identifier application number: M017 Numbing Cream MENTHOL FlexiGo Inc 41571c8f-332b-f423-e063-6394a90a8897 2025-10-20 Warnings Exact identifier application number: M017 Soothing Nerve Therapy MENTHOL Wise Consumer Products 40829d6b-5005-7ec9-e063-6294a90a970e 2025-10-20 Warnings Exact identifier application number: M017 Numbing Cream MENTHOL FlexiGo Inc 4146fd51-b18c-393d-e063-6294a90a4d9a 2025-10-20 Warnings Exact identifier application number: M017 Lidocaine 4% Maximum OTC Strength LIDOCAINE Cardinal Health 107, LLC 975031df-d46d-4098-b1c0-1c0c92b41995 2025-10-20 Warnings Exact identifier application number: M017 Cortizone 10 Intensive Healing HYDROCORTISONE Chattem, Inc. bb3d1a3e-4c0c-4694-9c05-80152dd9bd1c 2025-10-20 Warnings Exact identifier application number: M017 Sting relief pad BENZOCAINE, ALCOHOL Guangdong Comfort Medical Products Co., Ltd. 6e905065-10a9-1ded-e053-2a91aa0a46a1 2025-10-19 Warnings Exact identifier application number: M017 Elgin Pain Relief MENTHOL Eco-Logics, Inc. 375bfe83-c895-3ea7-e054-00144ff88e88 2025-10-18 Warnings Exact identifier application number: M017 Advanced Healing Diabetic Skin Care DIMETHICONE Eco-Logics, Inc. c6704d06-0311-406e-98a7-b8c8881aefd5 2025-10-18 Warnings Exact identifier application number: M017 Elgin Pain Relief MENTHOL Eco-Logics, Inc. 378d1109-6511-1f63-e054-00144ff88e88 2025-10-18 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 52241-100-03 52241010003 1 JAR in 1 CARTON (52241-100-03) / 3 g in 1 JAR 1 jar 2010-05-24 0000-00-00 No No Current 52241-100-10 52241010010 1 JAR in 1 CARTON (52241-100-10) / 10 g in 1 JAR 1 jar 2010-05-24 0000-00-00 No No Current 52241-100-30 52241010030 1 BOTTLE in 1 CARTON (52241-100-30) / 30 g in 1 BOTTLE 1 bottle 2010-05-24 0000-00-00 No No Current