Menthol

Product NDC
36800-252
Requested package NDC
36800-252-10
11-digit product format
368000252
Labeler code
36800
Product ID
36800-252_5ccea69a-bfc7-4068-e063-6394a90a177b
Type
HUMAN OTC DRUG
Nonproprietary name
Maximum Strength Medicated Foot Powder Talc Free
Dosage form
POWDER
Route
TOPICAL
Labeler
Topco Associates LLC
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2019-02-10
Substance
MENTHOL
Active strength
2.8 g/283g
NDC exclude flag
No
Listing certified through
2027-12-31
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 · 1 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2022-08-30 03:57 UTC · source 2022-08-29excluded packagepackage36800-25236800-252-10IInactivated by FDAexcluded / ndc_excluded.zipfb8cb913e6d1…eb8c232b6be0…

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
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL2.8 g/283g

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
36800-252-10Menthol283 g in 1 BOTTLE, PLASTICPOWDER2837

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
36800-252MENTHOL (MAXIMUM STRENGTH MEDICATED FOOT POWDER TALC FREE) POWDER [TOPCO ASSOCIATES LLC]6Current NDC, Legacy NDC, 1 package rows20241213_7caef8db-a07a-6705-e053-2991aa0aa724.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 20 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Stud 100 Male Genital DesensitizerLIDOCAINEPound International Corpd075656e-b13f-4a1d-bbb6-501e642698d52026-05-12WarningsExact identifier
application number: M017
CeraVe Developed with Dermatologists Itch Relief MoisturizingPRAMOXINE HYDROCHLORIDEL'Oreal USA Products Inc13ce57d0-b1c5-4685-ad7d-a562d9d8fc862026-05-12WarningsExact identifier
application number: M017
Calamine Plus Pramoxine HClCALAMINE PLUS SPRAYCVS Pharmacydb6f518d-3a0e-43f8-8d19-7382d9b7ff1c2026-05-11WarningsExact identifier
application number: M017
Cool and HeatMENTHOLAMERISOURCE BERGENf2bb0e8e-c4cd-0e8c-e053-2995a90a6df72026-05-11WarningsExact identifier
application number: M017
Instaflex Extra Strength Pain Relief CreamMENTHOL, METHYL SALICYLATEHealthy Directions, LLCd058c64d-0e4f-45aa-8f52-804961b562e32026-05-11WarningsExact identifier
application number: M017
BonicaEaseX Hot Capsicum Pain RelievingCAPSICUMPlanet (Anhui) Pharmaceutical Co.,Ltdca6e48af-af6d-4808-a576-0319d2080d382026-05-11WarningsExact identifier
application number: M017
BonicaEaseX Pain Relieving LidocaineLIDOCAINEPlanet (Anhui) Pharmaceutical Co., Ltd.7486fe89-a377-4a37-997d-e3bd16b891a72026-05-11WarningsExact identifier
application number: M017
YYSDMVY NUMBING CreamLIDOCAINE 4% NUMBING CREAMJiangxi Yudexi Pharmaceutical Co., LTD5195f5ec-8524-77f5-e063-6294a90abdc22026-05-11WarningsExact identifier
application number: M017
Lightning X Burn Relief GelLIDOCAINE HYDROCHLORIDENantong Health & Beyond Hygienic Products Inc.515eb4cc-63af-c11d-e063-6294a90a13ca2026-05-09WarningsExact identifier
application number: M017
Albertson Lidocaine, Menthol Pain Relief Medicated PatchLIDOCAINE AND MENTHOLSafewaydc647647-90ec-6beb-e053-2a95a90a79822026-05-09WarningsExact identifier
application number: M017
5 Elementum Lidocaine Male Genital DesensitizerLIDOCAINE MALE GENITAL DESENSITIZERMSVENTURESGROUP O514b1738-886e-a95d-e063-6294a90aa7072026-05-08WarningsExact identifier
application number: M017
Kroger Muscle Rub CreamMENTHOL, CAMPHOR, METHYL SALICYLATEKroger Co.45c8c79a-b4b4-d4be-e063-6394a90a92512026-05-08WarningsExact identifier
application number: M017
Walmart Equate Aloe Sunburn Relief CoolingLIDOCAINEWAL-MART STORES INC.51540f6b-596f-bc47-e063-6294a90a46ae2026-05-08WarningsExact identifier
application number: M017
Capsaicin 0.035% creamCAPSAICINMedcore LLC0236e1e4-c26c-4fff-a83b-143ce26d93bf2026-05-07WarningsExact identifier
application number: M017
Lidocaine 4% CreamLIDOCAINEMedcore LLC111cb421-ba3b-4772-ab60-d31eb41831682026-05-07WarningsExact identifier
application number: M017
Lidocaine 5% CreamLIDOCAINEMedcore LLC15d02b42-bf8b-486a-a081-f6d17cc11ec72026-05-07WarningsExact identifier
application number: M017
JenGufun LIDOCAINE Pain Relief Gel-PatchLIDOCAINE PAIN RELIEF GEL-PATCHHenan Kangdi Medical Devices Co., Ltd.51363a41-5dcc-6a3b-e063-6294a90a6c272026-05-07WarningsExact identifier
application number: M017
LidoxiLIDOCAINET&T Pharma Holdings LLC513c517e-c098-02aa-e063-6294a90ac8a42026-05-07WarningsExact identifier
application number: M017
Harris Teeter HydrocortisoneHYDROCORTISONEHARRIS TEETER LLC4e8199f8-96ec-5342-e063-6294a90afb2d2026-05-07WarningsExact identifier
application number: M017
CAREALL Hydrocortisone Maximum StrengthHYDROCORTISONENew World Imports, Inc.5114cdba-96a1-c399-e063-6294a90aac122026-05-06WarningsExact identifier
application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
259579menthol 1 % Topical PowderPSN7caef8db-a07a-6705-e053-2991aa0aa7247
259579menthol 0.01 MG/MG Topical PowderSCD7caef8db-a07a-6705-e053-2991aa0aa7247
259579menthol 1 % Topical PowderSY7caef8db-a07a-6705-e053-2991aa0aa7247

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
36800-252-1036800025210283 g in 1 BOTTLE, PLASTIC (36800-252-10) 283 g2019-02-100000-00-00NoNoCurrent