Menthol

Product NDC
62212-252
Requested package NDC
62212-252-03
11-digit product format
622120252
Labeler code
62212
Product ID
62212-252_28656961-9c32-9983-e063-6394a90ae6e4
Type
HUMAN OTC DRUG
Nonproprietary name
Amish Origins Medicated
Dosage form
CREAM
Route
TOPICAL
Labeler
Amish Origins LLC
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2013-01-01
Substance
MENTHOL
Active strength
8 g/100g
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
MENTHOL8 g/100g

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
727161Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
547abe39-3af3-4d70-99dd-caf8d67feda2Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62212-252-01Menthol99.22 g in 1 BOTTLECREAM99.2226
62212-252-02Menthol99.22 g in 1 BOTTLE, PUMPCREAM99.2226
62212-252-03Menthol400 g in 1 BOTTLECREAM40026
62212-252-04Menthol198.45 g in 1 BOTTLE, PUMPCREAM198.4526

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
MENTHOLACTIVE INGREDIENTL7T10EIP3AMENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]5
MENTHOLACTIVE MOIETYL7T10EIP3AMENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]5
ABIES SIBIRICA LEAF OILINACTIVE INGREDIENTXRY0V4VZKZMENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]5
ALOE VERA LEAFINACTIVE INGREDIENTZY81Z83H0XMENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]5
CAPRYLYL GLYCOLINACTIVE INGREDIENT00YIU5438UMENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]5
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2)INACTIVE INGREDIENTV2W71V8T0XMENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]5
CHLORPHENESININACTIVE INGREDIENTI670DAL4SZMENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]5
CINNAMOMUM CAMPHORA WHOLEINACTIVE INGREDIENT0B27814T7XMENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]5
EUCALYPTUS GLOBULUS LEAFINACTIVE INGREDIENTS546YLW6E6MENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]5
HYDROGENATED CASTOR OILINACTIVE INGREDIENTZF94AP8MEYMENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]5
METHYL SALICYLATEINACTIVE INGREDIENTLAV5U5022YMENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]5
PHENOXYETHANOLINACTIVE INGREDIENTHIE492ZZ3TMENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]5
SAFFLOWER OILINACTIVE INGREDIENT65UEH262ISMENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]5
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XMENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]5
SUNFLOWER SEED OIL GLYCERETH-8 ESTERSINACTIVE INGREDIENT358X17CAT0MENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]5
WATERINACTIVE INGREDIENT059QF0KO0RMENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62212-252MENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]26Current NDC, Legacy NDC, 4 package rows20241207_547abe39-3af3-4d70-99dd-caf8d67feda2.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 142 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Lidocaine Pain Relief Roll-OnLIDOCAINE 4%Humco Holding Group, Inc.a8be9e46-1616-40a9-e053-2a95a90ac3bc2023-12-15WarningsExact identifier
application number: M017
Hot/Cold Menthol 16% Roll-OnHOT/COLD MENTHOL 16% ROLL-ONHumco Holding Group, Inca8bf9744-9979-13c1-e053-2a95a90a30aa2023-12-15WarningsExact identifier
application number: M017
Freds Medicated anti itchPRAMOXINE HYDROCHLORIDE, MENTHOLDiscount Drug Mart8697b932-da5a-717e-e053-2a91aa0afcae2023-12-12WarningsExact identifier
application number: M017
CVS Medicated anti itchPRAMOXINE HYDROCHLORIDE, MENTHOLCVS86972218-31fe-6942-e053-2991aa0a88502023-12-12WarningsExact identifier
application number: M017
Best Choice Medicated anti itchPRAMOXINE HYDROCHLORIDE, MENTHOLvalue merchandisers869631f8-aa1e-8ea4-e053-2a91aa0a5c572023-12-12WarningsExact identifier
application number: M017
HydrocortisoneHYDROCORTISONE 1%Weeks & Leo Co., Inc.0c5325e3-4796-856c-e063-6394a90a1f902023-12-12WarningsExact identifier
application number: M017
Westlake Anti-itchHYDROCORTISONEWestlake Pharma LLC0c53c982-3f23-a2d5-e063-6394a90acd552023-12-12WarningsExact identifier
application number: M017
Rite Aid Anti-itchHYDROCORTISONERite Aid0c540422-1579-9217-e063-6294a90ad06a2023-12-12WarningsExact identifier
application number: M017
Anti-itch Paraben FreeHYDROCORTISONEWeeks & Leo Co., Inc.0c5419c5-0929-7ca6-e063-6294a90ac0a72023-12-12WarningsExact identifier
application number: M017
Rite Aid HydrocortisoneHYDROCORTISONE 1%Rite Aid0c580f96-7fe9-19df-e063-6394a90a5a222023-12-12WarningsExact identifier
application number: M017
Anti itchHYDROCORTISONEWeeks & Leo Co., Inc.0c58b750-d3a6-5ed1-e063-6294a90a43212023-12-12WarningsExact identifier
application number: M017
Greencaine BlastLIDOCAINEALMA Laboratories, Inc.031e0065-4c8a-43d8-bc69-3efa3c6c0ae32023-12-12WarningsExact identifier
application number: M017
Ageless Pain ReliefMETHYL SALICYLATE, MENTHOLIsagenix International, LLC3c7e493b-923d-44b1-9076-46c7894308d42023-12-12Warnings, Adverse reactionsExact identifier
application number: M017
CVS Extra Strength Itch StoppingDIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATECVS857af609-9dd7-a07a-e053-2991aa0ab6ba2023-12-11WarningsExact identifier
application number: M017
Rite Aid Extra Strength Itch StoppingDIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATERite Aid0c4170dd-e1fa-d549-e063-6394a90a5c232023-12-11WarningsExact identifier
application number: M017
Westlake Itch ReliefDIPHENHYDRAMINE HCL, ZINC ACETATEWestlake HB Pharma LLC0c416ba6-b01f-0609-e063-6294a90ae2a12023-12-11WarningsExact identifier
application number: M017
CVS Regular Strength Itch StoppingDIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATECVS87473ace-d834-e43f-e053-2a95a90a819c2023-12-11WarningsExact identifier
application number: M017
Katinko External Analgesic OilCAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATEGreenstone Pharmaceutical Inc.5881fc35-3293-4f0b-801a-afcd6feb94962023-12-08WarningsExact identifier
application number: M017
Katinko Pain And Itch RelievingCAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATEGreenstone Pharmaceutical Inc.fe907fa4-4a01-4974-b71f-9cd980b4eaa22023-12-08Warnings, Adverse reactionsExact identifier
application number: M017
CycleMENTHOLLa Mend, Inc.cfc0bcde-ef91-1e6c-e053-2a95a90ab79e2023-12-07WarningsExact identifier
application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
727161menthol 8 % Topical CreamPSN547abe39-3af3-4d70-99dd-caf8d67feda226
727161menthol 80 MG/ML Topical CreamSCD547abe39-3af3-4d70-99dd-caf8d67feda226
727161menthol 8 % Topical CreamSY547abe39-3af3-4d70-99dd-caf8d67feda226

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
62212-252-0362212025203400 g in 1 BOTTLE (62212-252-03) 400 g2013-01-01NoNoCurrent