Home NDC 75638-010 Doctor Hoys Pain Relief Gel
Product NDC 75638-010
11-digit product format 756380010
Labeler code 75638
Product ID 75638-010_4769df6d-225f-5a0d-e063-6394a90af652
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL, CAMPHOR (SYNTHETIC)
Dosage form GEL
Route TOPICAL
Labeler Dynamic Blending Specialists, Inc.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-03-01
Marketing end 2028-04-13
Substance MENTHOL; CAMPHOR (SYNTHETIC)
Active strength 50; 50 mg/mL; mg/mL
NDC exclude flag No
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 · 15 matching rows.
View current auxiliary records. · View the auxiliary file history.
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 Doctor Hoys Pain Relief Gel Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 50 mg/mL CAMPHOR (SYNTHETIC) 50 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L7T10EIP3A Internal UNII lookup 5TJD82A1ET Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 797500 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 75638-010-00 Doctor Hoys Pain Relief Gel 89 mL in 1 TUBE GEL 89 4 75638-010-01 Doctor Hoys Pain Relief Gel 177 mL in 1 TUBE GEL 177 4 75638-010-02 Doctor Hoys Pain Relief Gel 946 mL in 1 TUBE GEL 946 4 75638-010-03 Doctor Hoys Pain Relief Gel 1893 mL in 1 TUBE GEL 1893 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 75638-010 DOCTOR HOYS PAIN RELIEF GEL (MENTHOL, CAMPHOR (SYNTHETIC)) GEL [DYNAMIC BLENDING SPECIALISTS, INC.] 3 Current NDC, 4 package rows 20250201_50123bb9-d5d8-4ba6-ab94-8ed95fe0f5a8.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 124 of 151 · 3,020 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Fast Freeze Lidocaine Roll-On LIDOCAINE HYDROCHLORIDE, BENZYL ALCOHOL Natural Essentials, Inc. 74b06366-5eb4-4eba-aa2b-2b672828294d 2024-10-04 Warnings Exact identifier application number: M017 Fast Freeze Lidocaine LIDOCAINE Natural Essentials, Inc. 029bd3fb-1b5b-48e0-b9af-d91d548b5b0f 2024-10-04 Warnings Exact identifier application number: M017 Fast Freeze MENTHOL Natural Essentials Inc. a96e3e41-871c-4cf3-93b6-af2a6246ded8 2024-10-04 Warnings Exact identifier application number: M017 CVS Pain Relief MENTHOL 4% CVS 20234356-5e80-b79e-e063-6294a90a2ee3 2024-10-04 Warnings Exact identifier application number: M017 FLANAX BACK PAIN RELIEF LIDOCAINE Belmora Llc af4bf57c-f250-4506-83eb-e0f253e96062 2024-10-04 Warnings Exact identifier application number: M017 topcare hydrocortisone HYDROCORTISONE Topco Associates LLC 11a30ec9-ebc2-4a00-8a8d-431d0d973b37 2024-10-03 Warnings Exact identifier application number: M017 pain relief patch LIDOCAINE 4% Bionpharma Inc. 19c69983-4e78-8ec5-e063-6394a90a84be 2024-10-03 Warnings Exact identifier application number: M017 Good Sense Anti Itch HYDROCORTISONE L. Perrigo Company ecd6d841-40b9-42c9-825d-d172cd04824d 2024-10-03 Warnings Exact identifier application number: M017 Gold Bond Medicated Original Strength Body MENTHOL Navajo Manufacturing Company Inc. f71d598c-92c3-d6fd-e053-6394a90a97d7 2024-10-03 Warnings Exact identifier application number: M017 Signature Care Hydrocortisone HYDROCORTISONE Safeway 9e663535-4acc-4b37-acae-8c17517c5a3d 2024-10-03 Warnings Exact identifier application number: M017 Topcare Hydrocortisone HYDROCORTISONE Topco Associates LLC 849c60fc-e455-4c50-8adf-ac59c0ee785b 2024-10-03 Warnings Exact identifier application number: M017 rexall anti itch maximum strength relief HYDROCORTISONE Dolgencorp, LLC 894cf9ab-693a-4210-96df-605947f51b63 2024-10-03 Warnings Exact identifier application number: M017 equaline anti itch maximum strength HYDROCORTISONE United Natural Foods, Inc. dba UNFI 070000d7-7d4d-439b-9a91-851ba7c027e6 2024-10-03 Warnings Exact identifier application number: M017 hydrocortisone anti itch HYDROCORTISONE H E B a1a9fed8-4938-48b5-81f1-d3942d534bb8 2024-10-03 Warnings Exact identifier application number: M017 equaline anti itch HYDROCORTISONE United Natural Foods, Inc. dba UNFI ef9ea069-9b97-4bf5-aaac-deb85334dbd0 2024-10-03 Warnings Exact identifier application number: M017 Basic Care Hydrocortisone HYDROCORTISONE Amazon.com Services LLC 7fa13ab4-5f2d-4a48-816f-1b22d5f757b2 2024-10-03 Warnings Exact identifier application number: M017 hydrocortisone HYDROCORTISONE A-S Medication Solutions dc388dc1-0c4f-4bf1-8a12-fa39892317bc 2024-10-02 Warnings Exact identifier application number: M017 Geliga Muscular MENTHOL, METHYL SALICYLATE PT. EAGLE INDO PHARMA fb2beb08-0ad6-a89d-e053-6294a90aa6fe 2024-10-02 Warnings Exact identifier application number: M017 Geliga Muscular Balm MENTHOL, METHYL SALICYLATE PT. EAGLE INDO PHARMA da28097f-4b5c-6159-e053-2a95a90a7d96 2024-10-02 Warnings Exact identifier application number: M017 Circatrix CAPSAICIN PureTek Corporation cd3b1256-2df8-dc26-e053-2a95a90ad049 2024-10-02 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 75638-010-00 75638001000 89 mL in 1 TUBE (75638-010-00) 89 ml 2023-03-01 2028-04-13 No No Historical 75638-010-01 75638001001 177 mL in 1 TUBE (75638-010-01) 177 ml 2023-03-01 2028-01-24 No No Historical 75638-010-02 75638001002 946 mL in 1 TUBE (75638-010-02) 946 ml 2023-03-01 2028-01-24 No No Historical 75638-010-03 75638001003 1893 mL in 1 TUBE (75638-010-03) 1893 ml 2023-03-01 2028-01-24 No No Historical