Home NDC 75638-010-01 Doctor Hoys Pain Relief Gel
Product NDC 75638-010
Requested package NDC 75638-010-01
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 · 3 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 75638-010 75638-010-01 U Excluded because listing certification expired excluded / ndc_excluded.zip 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 75638-010 75638-010-01 U Excluded because listing certification expired excluded / ndc_excluded.zip ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 75638-010 75638-010-01 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…
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 18 of 152 · 3,029 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 75638-010-01 75638001001 177 mL in 1 TUBE (75638-010-01) 177 ml 2023-03-01 2028-01-24 No No Historical