FDA.reportPublic FDA data

Menthol Pain Relief Gel-Tube

Product NDC
83602-323
11-digit product format
836020323
Labeler code
83602
Product ID
83602-323_2d87bc23-69f4-511b-e063-6394a90ac880
Type
HUMAN OTC DRUG
Nonproprietary name
Menthol
Dosage form
GEL
Route
TOPICAL
Labeler
Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2023-12-06
Substance
MENTHOL
Active strength
.04 g/mL
Listing certified through
2026-12-31
Current FDA listing
Yes

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 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct83602-323DDiscontinued by firm2026-10-20
excluded packagepackage83602-32383602-323-30DDiscontinued by firm2026-10-20

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
Menthol Pain Relief Gel-Tube
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL.04 g/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
L7T10EIP3AInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
415974Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
0bb07892-824e-8691-e063-6294a90a3891Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83602-323-30Menthol Pain Relief Gel-Tube89 mL in 1 TUBEGEL895

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83602-323MENTHOL PAIN RELIEF GEL-TUBE (MENTHOL) GEL [GUANGZHOU LIUQUANMIAO IMPORT & EXPORT TRADE CO., LTD.]51 package rows20250209_0bb07892-824e-8691-e063-6294a90a3891.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 128 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AOSI HEALTHCARE BURNLIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDENantong Health & Beyond Hygienic Products Inc.a28b920c-0bb8-4b5a-addd-26ea164e036e2024-09-25WarningsExact identifier
application number: M017
anti itchDIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATEKroger Company067e718a-ec0b-4895-8f9f-82d64ab4c7b42024-09-24WarningsExact identifier
application number: M017
topcare anti itchDIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATETopco Associates LLCe0fb332a-2903-41ef-b35b-7cd3a74cff992024-09-24WarningsExact identifier
application number: M017
equaline anti itchHYDROCORTISONEUnited Natural Foods, Inc. dba UNFI83cd9f60-a4c4-4dea-97a7-cd96aade9e882024-09-24WarningsExact identifier
application number: M017
good sense itch reliefDIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATEL. Perrigo Company162fe0a3-3995-4e6f-94ed-f839b2b0c80e2024-09-24WarningsExact identifier
application number: M017
Caring Mill Anti-Itch CreamDIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATEVeridian Healthcare22ca137a-576c-a13c-e063-6394a90ae7fc2024-09-23WarningsExact identifier
application number: M017
Signature Care Anti ItchHYDROCORTISONESafewayed0eb068-3ce6-423d-a7f8-c3456b7f60402024-09-23WarningsExact identifier
application number: M017
members mark hydrocortisoneHYDROCORTISONESam's West Inc218f0dcd-fa67-4935-8019-ecbbd53ed2f72024-09-23WarningsExact identifier
application number: M017
anti itchHYDROCORTISONEMeijer, Inc.a07496e0-6fc2-4190-8a01-f513134ffb922024-09-23WarningsExact identifier
application number: M017
ZYLOTROL PAIN RELIEVINGLIDOCAINE HCL, MENTHOLWhitestone Products LLC2301fed7-0fa9-450d-8b1b-006f53235be02024-09-21WarningsExact identifier
application number: M017
Tibetree Cheezheng Joint Analgesic PatchCAMPHORTibet Cheezheng Tibetan Medicine Co. Ltd65a8a63f-1864-473e-be72-7840a6a5dee72024-09-20WarningsExact identifier
application number: M017
Cold Ice Analgesic GelMENTHOLDabur India Limited22915b2f-5f76-3e38-e063-6394a90a07b42024-09-20WarningsExact identifier
application number: M017
Exchange Select HydrocortisoneHYDROCORTISONEArmy & Air Force Exchange Service1b709db3-7dc1-4756-a8a0-dddda875dc572024-09-19WarningsExact identifier
application number: M017
Theraworx PM Nighttime Maximum Strength Pain ReliefLIDOCAINE HYDROCHLORIDEAVADIM HOLDINGS, INC.bc8cb476-9a47-47b3-ad78-a6ecec9ee66f2024-09-19WarningsExact identifier
application number: M017
LidocaineLIDOCAINEStratus Pharmaceuticals Ince1a8d4a7-01f7-4bab-8d09-875c461b3b612024-09-19WarningsExact identifier
application number: M017
Camphor SpiritCAMPHOR 10%Strategic Sourcing Services, LLC2216d799-7f6f-cab7-e063-6294a90a8d6c2024-09-14WarningsExact identifier
application number: M017
Meijer Analgesic Lidocaine Topical AnalgesicLIDOCAINE HYDROCHLORIDEMeijer Distribution, Incf5d39be6-3b91-4ba1-9015-fd3ffbbdf4aa2024-09-12WarningsExact identifier
application number: M017
leader anti itchDIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATECardinal Health 110, LLC. dba Leadere1aab35b-80d9-4515-afb7-8c662bc5d0282024-09-11WarningsExact identifier
application number: M017
LactiGoMENTHOLLactiGo, Inc.849c3601-2bc8-0991-e053-2a91aa0a5e7f2024-09-03WarningsExact identifier
application number: M017
Hempvana Ultra Strength Pain Relief Gel Platinum - ArthritisMENTHOL 8%Telebrands Corpc22cf1a5-0d5d-5ea5-e053-2995a90a333b2024-09-02WarningsExact identifier
application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
415974menthol 4 % Topical GelPSN0bb07892-824e-8691-e063-6294a90a38915
415974menthol 0.04 MG/MG Topical GelSCD0bb07892-824e-8691-e063-6294a90a38915
415974menthol 4 % Topical GelSY0bb07892-824e-8691-e063-6294a90a38915

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleStatus
83602-323-308360203233089 mL in 1 TUBE (83602-323-30)89 ml2023-12-060Current