FDA.reportPublic FDA data

Doctor Hoys Natural Pain Relief

Product NDC
10842-102
Requested package NDC
10842-102-01
11-digit product format
108420102
Labeler code
10842
Product ID
10842-102_ef195bfa-447b-e58b-e053-2a95a90a7073
Type
HUMAN OTC DRUG
Nonproprietary name
camphor, menthol
Dosage form
GEL
Route
TOPICAL
Labeler
DOCTOR HOY'S, LLC
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2005-05-10
Marketing end
0000-00-00
Substance
CAMPHOR (NATURAL); MENTHOL
Active strength
50 mg/mL; mg/mL
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage10842-10210842-102-01IInactivated by FDA2026-10-05

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.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…
2024-05-28 21:12 UTC · source 2024-05-288af77b9d5b6f…d9bbb34c5368…
2024-05-15 03:39 UTC · source 2024-05-14834df4deac94…adcc014656a3…
2024-03-11 06:39 UTC · source 2024-03-081332a3947898…d4bfe170f9cd…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Related label table
NDCRelated label
10842-102-01Pain Relief Gel
10842-102-02Pain Relief Gel
10842-102-03Pain Relief Gel
10842-102-04Pain Relief Gel
10842-102-05Pain Relief Gel
10842-102-08Pain Relief Gel
10842-102-09Pain Relief Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10842-102-01Doctor Hoys Natural Pain Relief237 mL in 1 BOTTLE, DISPENSINGGEL23719
10842-102-02Doctor Hoys Natural Pain Relief1814 mL in 1 JUGGEL181419
10842-102-03Doctor Hoys Natural Pain Relief118 mL in 1 TUBEGEL11819
10842-102-04Doctor Hoys Natural Pain Relief5 mL in 1 PACKETGEL519
10842-102-05Doctor Hoys Natural Pain Relief946 mL in 1 JUGGEL94619
10842-102-08Doctor Hoys Natural Pain Relief89 mL in 1 BOTTLE, WITH APPLICATORGEL8919
10842-102-09Doctor Hoys Natural Pain Relief3785 mL in 1 JUGGEL378519

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CAMPHOR (NATURAL)ACTIVE INGREDIENTN20HL7Q941DOCTOR HOYS NATURAL PAIN RELIEF (MENTHOL, CAMPHOR) GEL [DOCTOR HOY'S, LLC]6
MENTHOLACTIVE INGREDIENTL7T10EIP3ADOCTOR HOYS NATURAL PAIN RELIEF (MENTHOL, CAMPHOR) GEL [DOCTOR HOY'S, LLC]6
CAMPHOR (NATURAL)ACTIVE MOIETYN20HL7Q941DOCTOR HOYS NATURAL PAIN RELIEF (MENTHOL, CAMPHOR) GEL [DOCTOR HOY'S, LLC]6
MENTHOLACTIVE MOIETYL7T10EIP3ADOCTOR HOYS NATURAL PAIN RELIEF (MENTHOL, CAMPHOR) GEL [DOCTOR HOY'S, LLC]6
ARNICA MONTANAINACTIVE INGREDIENTO80TY208ZWDOCTOR HOYS NATURAL PAIN RELIEF (MENTHOL, CAMPHOR) GEL [DOCTOR HOY'S, LLC]6
ISOPROPYL ALCOHOLINACTIVE INGREDIENTND2M416302DOCTOR HOYS NATURAL PAIN RELIEF (MENTHOL, CAMPHOR) GEL [DOCTOR HOY'S, LLC]6
WATERINACTIVE INGREDIENT059QF0KO0RDOCTOR HOYS NATURAL PAIN RELIEF (MENTHOL, CAMPHOR) GEL [DOCTOR HOY'S, LLC]6
WITCH HAZELINACTIVE INGREDIENT101I4J0U34DOCTOR HOYS NATURAL PAIN RELIEF (MENTHOL, CAMPHOR) GEL [DOCTOR HOY'S, LLC]6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10842-102DOCTOR HOYS NATURAL PAIN RELIEF (CAMPHOR, MENTHOL) GEL [DOCTOR HOY'S, LLC]19Legacy NDC, 7 package rows20221206_898f7784-693f-46f6-a9ac-778e0e6aa3b6.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
797500camphor 5 % / menthol 5 % Topical GelPSN898f7784-693f-46f6-a9ac-778e0e6aa3b619
797500camphor 0.05 MG/MG / menthol 0.05 MG/MG Topical GelSCD898f7784-693f-46f6-a9ac-778e0e6aa3b619
797500camphor 5 % / menthol 5 % Topical GelSY898f7784-693f-46f6-a9ac-778e0e6aa3b619
797500camphor 5 % / menthol 5 % Topical GelPSN87b0edfe-e929-147f-e053-2a95a90aed2515
797500camphor 0.05 MG/MG / menthol 0.05 MG/MG Topical GelSCD87b0edfe-e929-147f-e053-2a95a90aed2515
797500camphor 5 % / menthol 5 % Topical GelSY87b0edfe-e929-147f-e053-2a95a90aed2515

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
10842-102-0110842010201237 mL in 1 BOTTLE, DISPENSING (10842-102-01) 237 ml2005-05-100000-00-00NoNoCurrent