Menthol

Product NDC
81522-069
11-digit product format
815220069
Labeler code
81522
Product ID
81522-069_422aaf23-440e-34a8-e063-6294a90a215d
Type
HUMAN OTC DRUG
Nonproprietary name
Maximum Strength Medicated Foot Powder Talc Free
Dosage form
POWDER
Route
TOPICAL
Labeler
FSA Store Inc.
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2023-05-02
Substance
MENTHOL
Active strength
10 mg/g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

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
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL10 mg/g

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
259579Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
fb3548c8-f202-dc50-e053-6394a90a5b30Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81522-069-01Menthol283 g in 1 BOTTLE, PLASTICPOWDER2834

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81522-069MENTHOL (MAXIMUM STRENGTH MEDICATED FOOT POWDER TALC FREE) POWDER [FSA STORE INC.]3Current NDC, 1 package rows20241109_fb3548c8-f202-dc50-e053-6394a90a5b30.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 12 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Natures Willow Balm Roll On Pain ReliefMENTHOLWB Ventures LLC3b1834e6-75cd-5380-e063-6294a90ad1d52026-07-08WarningsExact identifier
application number: M017
Natures Willow Balm Itch Relief CreamMENTHOLWB Ventures LLC0ce31b5d-4401-460c-e063-6394a90ab5582026-07-08WarningsExact identifier
application number: M017
CAREALL Hydrocortisone Maximum StrengthHYDROCORTISONENew World Imports, Inc.560a4abf-31dd-333f-e063-6294a90a35052026-07-08WarningsExact identifier
application number: M017
Natures Willow BalmMENTHOLWB VENTURES LLCb9f50c43-b0d5-39a8-e053-2995a90a04f12026-07-08WarningsExact identifier
application number: M017
Natures Willow Bug Bite BalmMENTHOLWB Ventures LLCb9fab18f-32c7-d5bd-e053-2995a90a6d0f2026-07-08WarningsExact identifier
application number: M017
Salonpas pain relieving hotCAPSAICIN, MENTHOLHisamitsu Pharmaceutical Co., Inc.d2aa8820-a947-404b-b617-e692fbd165022026-07-07WarningsExact identifier
application number: M017
Quali Yi Tiao Gen Pain PatchCAPSAICIN PATCHSheng Chang Pharmaceutical Co, Ltd. Zhongli Factory33154a9b-f6d0-4e95-b4cb-6b938f5dcf4d2026-07-07WarningsExact identifier
application number: M017
MUYOHON Numbing CreamNUMBING CREAMGuangzhou Jingliang Cosmetics Co., Ltd.55caf0a5-f062-a6c3-e063-6294a90ae0732026-07-04WarningsExact identifier
application number: M017
Targeted Warming Capsaicin PatchCAPSAICINArmy & Air Force Exchange Service55b539f8-38c4-594e-e063-6394a90afbaa2026-07-03WarningsExact identifier
application number: M017
TopCare Health Pain ReliefLIDOCAINE HYDROCHLORIDETopco Associates LLC485b0671-da09-19d7-e063-6294a90aca5d2026-07-03WarningsExact identifier
application number: M017
Mineral Ice Methol Pain ReliefMENTHOL 10.5 %Sunflora Inc6ddd9e97-f717-4d5a-9658-26449a3cc8312026-07-02WarningsExact identifier
application number: M017
Burn ReliefLIDOCAINEAmerisourceBergen Drug Corporation7d898e33-ded7-c9b9-e053-2a91aa0adf7c2026-07-01WarningsExact identifier
application number: M017
Desert Harvest Releveum with LidocaineLIDOCAINE HYDROCHLORIDEDesert Harvest, Inc9ad514ab-a6bd-4564-8ba3-0149032ebf362026-07-01WarningsExact identifier
application number: M017
CVS No Mess CortisoneHYDROCORTISONENatural Essentials, Inc.558c94ec-95f1-eb98-e063-6394a90a1e722026-07-01WarningsExact identifier
application number: M017
MUSCLE EASEMENTHOL CAMPHORSOMBRA COSMETICS INC.03fff4bf-04ed-49a6-b40f-4d98c2b42f692026-07-01WarningsExact identifier
application number: M017
OrthoNesic Pain Relieving GelMENTHOL, CAMPHORBlaine Labs Inc.122f60c2-f8df-4625-8bb8-a2244a261b5d2026-07-01WarningsExact identifier
application number: M017
Desert Harvest RELEVEUMLIDOCAINEDesert Harvest Inc.5d9010ec-d482-44ff-ba27-3bfec5a241c62026-06-30WarningsExact identifier
application number: M017
PromescentLIDICAINEAbsorption5b508238-3be7-4b0d-bf35-51de79f58f552026-06-30WarningsExact identifier
application number: M017
LidovyxLIDOCAINE 4%V2 Pharma LLC4465eb60-a617-4608-9504-8b3b4c64f49e2026-06-30WarningsExact identifier
application number: M017
Dr.Johnes Lidocaine 4% Topical Analgesic CreamLIDOCAINE HCL,MENTHOLDr.Johnes LLC6144708d-4b0f-4f0d-88e3-6925ba2d004d2026-06-29WarningsExact identifier
application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
259579menthol 1 % Topical PowderPSNfb3548c8-f202-dc50-e053-6394a90a5b304
259579menthol 0.01 MG/MG Topical PowderSCDfb3548c8-f202-dc50-e053-6394a90a5b304
259579menthol 1 % Topical PowderSYfb3548c8-f202-dc50-e053-6394a90a5b304

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
81522-069-0181522006901283 g in 1 BOTTLE, PLASTIC (81522-069-01) 283 g2023-05-02NoNoCurrent