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 110 of 152 · 3,029 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Dollar General Cold-Hot Medicated Patches MENTHOL DOLGENCORP, LLC c6e0388b-af9e-4e51-8f94-6788185c31a0 2024-12-18 Warnings Exact identifier application number: M017 THERA CARE PAIN THERAPY LIDOCAINE Veridian Healthcare e023bb5a-a4bc-4681-a1f4-48ca0d2cb102 2024-12-18 Warnings Exact identifier application number: M017 TheraCare Medicated Pain Relief Patches CAMPHOR, MENTHOL, METHYL SALICYLATE Veridian Healthcare f6f3c9c0-d6e3-75a3-e053-6294a90a1965 2024-12-18 Warnings Exact identifier application number: M017 Good Sense Hot and Cold Medicated Patch MENTHOL GOOD SENSE 1b16c3e5-a29f-4043-94e6-0a0e0ea3d93e 2024-12-18 Warnings Exact identifier application number: M017 Hunter Beach 4% LIDOCAINE HUNTERS BEACH LIFE f2ef9c12-6e42-486b-b6f2-0ad534e94294 2024-12-18 Warnings Exact identifier application number: M017 Hunter Beach 4% LIDOCAINE HUNTERS BEACH LIFE 05a9605b-0d01-4333-8e54-7202e7c31c49 2024-12-18 Warnings Exact identifier application number: M017 Ultra Strength Muscle Rub CAMPHOR, MENTHOL, METHYL SALICYLATE The Mentholatum Company 32b64985-0e2f-49ee-9840-946d7279fee7 2024-12-17 Warnings Exact identifier application number: M017 CVS Health Cold and Hot Pain Relieving Extra Strength MENTHOL, METHYL SALICYLATE CVS Pharmacy 1ca1a631-cb2c-46cd-bd41-05469b08d208 2024-12-17 Warnings Exact identifier application number: M017 Mentholatum Pain Relieving MENTHOL, METHYL SALICYLATE The Mentholatum Company 0056b952-9870-485a-9f35-f985472875a9 2024-12-17 Warnings Exact identifier application number: M017 Mentholatum Lidocaine Heat LIDOCAINE HCL The Mentholatum Company cc2ef25a-b569-4d48-a666-899f710b4b34 2024-12-17 Warnings Exact identifier application number: M017 Rite Aid Muscle Rub Ultra Strength CAMPHOR, MENTHOL, METHYL SALICYLATE Rite Aid Corporation 039fff40-b5ba-42cb-932c-8a70ca92759d 2024-12-17 Warnings Exact identifier application number: M017 Signature Care Cold and Hot Medicated MENTHOL Safeway 88f59f95-0a7c-458c-949c-0dff16ad94e4 2024-12-17 Warnings Exact identifier application number: M017 Equate Cool and Heat MENTHOL, METHYL SALICYLATE Wal-Mart Stores Inc c5ab2426-eeca-4ba4-9f00-7790d2176471 2024-12-17 Warnings Exact identifier application number: M017 CVS Health Muscle Rub Ultra Strength CAMPHOR, MENTHOL, METHYL SALICYLATE CVS Pharmacy 4fc0d6bb-efa7-40cf-a6d5-e0feaa93c80a 2024-12-17 Warnings Exact identifier application number: M017 DG Health Maximum Strength Pain Relieving Cleansing BENZALKONIUM CL, LIDOCAINE HCL Dollar General Corporation 64f69315-77a3-49dc-940d-efd7a29c6645 2024-12-17 Warnings Exact identifier application number: M017 Chiggerex BENZOCAINE RANDOB LABS, LTD. DBA CROSSINGWELL CONSUMER HEALTH 5e5d84ab-f57f-448d-a4c1-ced38890eec2 2024-12-17 Warnings Exact identifier application number: M017 DerMend Moisturizing Anti-Itch PRAMOXINE HYDROCHLORIDE Ferndale Laboratories, Inc. 14c7fb1c-a310-4b12-ab2e-7f1c0801995c 2024-12-17 Warnings Exact identifier application number: M017 Hydrocortisone 1% HYDROCORTISONE Geri-Care Pharmaceuticals, Corp fd67566a-1076-019d-e053-6394a90a415c 2024-12-17 Warnings Exact identifier application number: M017 Extra Strength MENTHOL AND METHYL SALICYLATE NATURES FORMULAE HEALTH PRODUCTS LTD. d919b50a-5de2-1830-e053-2a95a90ab88d 2024-12-17 Warnings Exact identifier application number: M017 Cold and Heat Lidocaine Patch Plus Menthol LIDOCAINE, MENTHOL Walgreen Company 1f262473-3f3c-4f3f-b507-590d06ff69a9 2024-12-17 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