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 130 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SANTO REMEDIO Alivio Pain Relieving Lavender ScentLIDOCAINE HYDROCHLORIDE, MENTHOLSANTO REMEDIO LLCab53c7f2-a768-4f36-89d6-e128a1a940c22024-08-05WarningsExact identifier
application number: M017
CVS Health Maximum Strength HydrocortisoneHYDROCORTISONE OINTMENTCVS Healthee9ed7ca-1642-4cf6-ae4b-d1c11b37eaf32024-08-02WarningsExact identifier
application number: M017
Anti-Itch Vulva Cream 1 Hydrocortisone AcetateHYDROCORTISONE ACETATEThe Honey Pot Company LLC6f32b536-6ebf-49a8-abb6-2a1daae2f6d72024-08-01WarningsExact identifier
application number: M017
Anti Itch Soothing 1 Pramoxine HydrochloridePRAMOXINE HYDROCHLORIDEThe Honey Pot Company LLC8bfeea34-25d5-4721-a17f-d9f1d0084cc32024-08-01WarningsExact identifier
application number: M017
AVON footworks Arthritis Achy Foot and MuscleMETHYL SALICYLATEThe Avon Company1f440f60-cfc4-511e-e063-6294a90a87db2024-08-01WarningsExact identifier
application number: M017
AVON footworks Maximum Strength Cracked HeelBENZALKONIUM CHLORIDE, LIDOCAINEThe Avon Company1f45752e-4a55-431e-e063-6294a90aa57a2024-08-01WarningsExact identifier
application number: M017
ReliefMENTHOLLa Mend, Inc.1f92de3a-7180-5884-e063-6294a90aebf52024-08-01WarningsExact identifier
application number: M017
Meijer Medicated Foot PowderMENTHOLMeijer Distribution07ec6c20-73c4-e5e4-e063-6294a90a7e552024-07-29WarningsExact identifier
application number: M017
Ralli Rapid Pain ReliefMENTHOLTroy Manufacturing, Inc.e05ec3b7-e9ab-4eaa-8518-86304336697c2024-07-29WarningsExact identifier
application number: M017
Walgreens Roll-OnCAPSAISIN 0.1%Walgreens Co1e65bf31-15c7-5e6a-e063-6394a90ac9562024-07-29WarningsExact identifier
application number: M017
CamphotrexCAMPHOR, MENTHOLPureTek Corporation3b6c6eef-e92d-497d-afe8-82356637c2b82024-07-26WarningsExact identifier
application number: M017
CamphotrolCAMPHOR, MENTHOLPureTek Corporationccac9f37-a374-4765-e053-2a95a90ad2f72024-07-26WarningsExact identifier
application number: M017
Real Time Pain Relief FootMENTHOLReal Time Products Inc.29c8e06d-9b29-44f9-ac21-9160d06475cb2024-07-24WarningsExact identifier
application number: M017
Capsaicin 0.075 PercentCAPSAICINAlexso, Inc33d2a9cd-0ca1-4e19-8b7a-f899f1205cbd2024-07-22WarningsExact identifier
application number: M017
TIDL Pain Relief CRYO Therapy Limited EditionPAIN RELIEF CRYO THERAPY LIMITED EDITIONShenzhen Sam Technology Co., Ltd.1d966b67-fd9c-eab6-e063-6294a90aa75e2024-07-19WarningsExact identifier
application number: M017
Fruit of the Earth Aloe Vera Cool BlueLIDOCAINE HYDROCHLORIDEFruit of the Earth, Inc.1d65bc34-2bc2-4f52-a9b3-1cb08324eb792024-07-19WarningsExact identifier
application number: M017
Ultra BalmMENTHOL AND METHYL SALICYLATELing Nam Medicine Factory (H.K.) Ltd.de997baf-aa04-474e-b912-3fc67e720d0b2024-07-19WarningsExact identifier
application number: M017
Ling Nam Hak Kwai OilTURPENTINE OILLing Nam Medicine Factory (H.K.) Ltd.3f16cce3-366f-41f3-8829-6de4082a8c192024-07-19WarningsExact identifier
application number: M017
Koong Yick Hak Kwai OilTURPENTINE OILLing Nam Medicine Factory (H.K.) Ltd.bc33e185-3b42-98b5-e053-2995a90a63082024-07-18WarningsExact identifier
application number: M017
Koong Yick Hung FaMETHYL SALICYLATELing Nam Medicine Factory (H.K.) Ltd.9c8a121d-6da2-4435-a2d7-a0b71d10740d2024-07-18WarningsExact 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