FDA.reportPublic FDA data

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 84 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SYNC ICESYNC RELIEF ICEiON Pharma, LLC38ce98ce-a7bf-8041-e063-6394a90ae7302025-07-28WarningsExact identifier
application number: M017
SYNC PROSYNC RELIEF PRO CREAMiON Pharma, LLC3a3e91d6-732b-dca9-e063-6394a90a06d42025-07-28WarningsExact identifier
application number: M017
Careland Pain ReliefMETHYL SALICYLATE, MENTHOLPlanet (Anhui) Pharmaceutical Co., Ltd.83f36771-1033-4fd0-a0e6-82c1dcfedeee2025-07-28WarningsExact identifier
application number: M017
Rite Aid anti-itchHYDROCORTISONERite Aid Corporation2a232dd1-9071-4c55-a7f7-19d8404b99a62025-07-28WarningsExact identifier
application number: M017
Hydrocortisone Plus 12 MoisturizersHYDROCORTISONERITE AID CORPORATION05598255-3e7a-46a5-ae7e-dcfcb616d59d2025-07-28WarningsExact identifier
application number: M017
Inked InspiredLIDOCAINE HCLProdigy Media Inc54fb2860-7e63-4598-953a-170226e613e92025-07-28WarningsExact identifier
application number: M017
Ujhay Hydrocortisone Ointment.UJHAY HYDROCORTISONE OINTMENTGuangdong Quadrant Ecological Technology Co., Ltd.3af59276-8e6a-0603-e063-6394a90a1f9b2025-07-27WarningsExact identifier
application number: M017
SANA SANA Menthol External AnalgesicMENTHOLAlquimia Najulam S de RL de CV8b7edd51-e08a-4e01-9df0-8305ce17b4182025-07-25WarningsExact identifier
application number: M017
Hydrocortisone Intensive Healing FormulaHYDROCORTISONETARGET Corporation682b737f-e453-4079-bf31-47a9485c78972025-07-25WarningsExact identifier
application number: M017
Chigg AwayBENZOCAINEPierson Laboratories, Inc.8372e7c1-f145-4bc5-85ab-cf831abe70ce2025-07-24WarningsExact identifier
application number: M017
Chigg AwayBENZOCAINEPharma Nobis, LLCe42fa1c6-d804-630f-e053-2995a90add6b2025-07-24WarningsExact identifier
application number: M017
Cannarelief 2000mgMENTHOLEarthmed LLC01f810de-52ba-8beb-e063-6394a90a61c02025-07-24WarningsExact identifier
application number: M017
CHING WAN HUNG SOOTHING HERBAL BALMMENTHOLTIANJIN DARENTANG JINGWANHONG PHARMACEUTICAL CO., LTD.ffadc904-8e9d-4cb8-815a-d583bbdb3f0b2025-07-24WarningsExact identifier
application number: M017
PT Elite Premium Pain ReliefCAPSAICIN, MENTHOLPT ELITE PRODUCTS LLCad251821-4c58-425d-bdcb-8dd9bd41b7132025-07-23WarningsExact identifier
application number: M017
Whipped Butter SPF 50ZINC OXIDEBloomeffects, Inc374b62d8-e012-591f-e063-6294a90aef932025-07-23WarningsExact identifier
application number: M017
Game On XtremeMENTHOL, UNSPECIFIED FORMNatural Essentials Inc.5a1b6192-d537-42b3-add8-22c63e7c986c2025-07-23WarningsExact identifier
application number: M017
AMRUTANJAN RELIEF PAIN BALMCAMPHOR , MENTHOL, METHYL SALICYLATEAMRUTANJAN HEALTH CARE LIMITEDddee6714-8b18-4d87-944b-8467fda22e6b2025-07-23WarningsExact identifier
application number: M017
Stopain Extra Strength GelMENTHOLTroy Manufacturing, Inc.8bb89002-d7a2-4bee-b5a5-1fd1949273ef2025-07-22WarningsExact identifier
application number: M017
Hielo ArdienteMENTHOLMenper Distributors, Inc.97ec516c-d2bc-47ce-82fe-bd68445d95702025-07-22WarningsExact identifier
application number: M017
La Flecha JaponesaMETHYL SALICYLATEMenper Distributors, Inc.08819ad0-97c2-49bd-b923-535b94a271672025-07-22WarningsExact 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