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
Ingredient	Strength
MENTHOL	8 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
L7T10EIP3A	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
727161	Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
Identifier	FDA.report destination
547abe39-3af3-4d70-99dd-caf8d67feda2	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
62212-252-01	Menthol	99.22 g in 1 BOTTLE	CREAM	99.22	26
62212-252-02	Menthol	99.22 g in 1 BOTTLE, PUMP	CREAM	99.22	26
62212-252-03	Menthol	400 g in 1 BOTTLE	CREAM	400	26
62212-252-04	Menthol	198.45 g in 1 BOTTLE, PUMP	CREAM	198.45	26

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	MENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]	5
MENTHOL	ACTIVE MOIETY	L7T10EIP3A	MENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]	5
ABIES SIBIRICA LEAF OIL	INACTIVE INGREDIENT	XRY0V4VZKZ	MENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]	5
ALOE VERA LEAF	INACTIVE INGREDIENT	ZY81Z83H0X	MENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]	5
CAPRYLYL GLYCOL	INACTIVE INGREDIENT	00YIU5438U	MENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]	5
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2)	INACTIVE INGREDIENT	V2W71V8T0X	MENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]	5
CHLORPHENESIN	INACTIVE INGREDIENT	I670DAL4SZ	MENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]	5
CINNAMOMUM CAMPHORA WHOLE	INACTIVE INGREDIENT	0B27814T7X	MENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]	5
EUCALYPTUS GLOBULUS LEAF	INACTIVE INGREDIENT	S546YLW6E6	MENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]	5
HYDROGENATED CASTOR OIL	INACTIVE INGREDIENT	ZF94AP8MEY	MENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]	5
METHYL SALICYLATE	INACTIVE INGREDIENT	LAV5U5022Y	MENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]	5
PHENOXYETHANOL	INACTIVE INGREDIENT	HIE492ZZ3T	MENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]	5
SAFFLOWER OIL	INACTIVE INGREDIENT	65UEH262IS	MENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]	5
SODIUM CHLORIDE	INACTIVE INGREDIENT	451W47IQ8X	MENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]	5
SUNFLOWER SEED OIL GLYCERETH-8 ESTERS	INACTIVE INGREDIENT	358X17CAT0	MENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]	5
WATER	INACTIVE INGREDIENT	059QF0KO0R	MENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62212-252	MENTHOL (AMISH ORIGINS MEDICATED) CREAM [AMISH ORIGINS LLC]	26	Current NDC, Legacy NDC, 4 package rows	20241207_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 138 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Joint and Muscle Pain	MENTHOL	Shaklee Corporation	3943824f-1f4f-4d6f-bd73-0b1be02162a5	2024-01-30	Warnings	Exact identifier application number: M017
Mirakel Pain Relief Roll-On	LIDOCAINE HCL	Sanvio, Inc.	102f3618-13ad-37e3-e063-6294a90a8086	2024-01-30	Warnings	Exact identifier application number: M017
Blistex Lip Medex	PETROLATUM, MENTHOL, UNSPECIFIED FORM, CAMPHOR (SYNTHETIC), AND PHENOL	Blistex Inc.	8ad39005-9419-4f1a-a1ae-2f76d212455e	2024-01-26	Warnings	Exact identifier application number: M017
Point Relief Cold Spot Pain Relieving	MENTHOL	Fabrication Enterprises	ad5d6f04-15e6-4548-95c2-32271c186bc1	2024-01-25	Warnings	Exact identifier application number: M017
MIND BODY MATRIX PAIN RELIEF	MENTHOL	Functional Energetic, Inc.	3667dd0d-942e-4101-ba98-cb013ae77cf5	2024-01-25	Warnings	Exact identifier application number: M017
SUPER WHITE STUFF Pain Relief	MENTHOL	BLUE SPRING WELLNESS	e6d27df5-118c-4c6d-86e8-7b4401a39c76	2024-01-23	Warnings	Exact identifier application number: M017
Burn First Aid	BURN FIRST AID	Dynarex Corporation	826e08be-dffa-5a27-e053-2a91aa0a8701	2024-01-22	Warnings	Exact identifier application number: M017
Target Up and Up Pain Relief Menthol Topical Analgesic Roll-On	MENTHOL	TARGET CORPORATION	0f95fc55-8665-9e89-e063-6394a90a7891	2024-01-22	Warnings	Exact identifier application number: M017
CVS Health Lidocaine Pain Relief Plus Menthol	LIDOCAINE, MENTHOL, UNSPECIFIED FORM	Natural Essentials, Inc.	77978069-a1b4-473e-83c9-8320e00eea89	2024-01-19	Warnings	Exact identifier application number: M017
ZIMS MAX FREEZE LEG CRAMPS	CAMPHOR, MENTHOL	KOBAYASHI Healthcare International, Inc.	ba26635d-95d3-4d88-93cc-1fd4fd29fd79	2024-01-18	Warnings	Exact identifier application number: M017
Burn	LIDOCAINE	HART Health	e95ebdac-9789-41c2-97da-2307e4538794	2024-01-18	Warnings	Exact identifier application number: M017
Medi-First Hydrocortisone 1%	HYDROCORTISONE ACETATE	Unifirst First Aid Corporation	bd216f5d-f304-7d8d-e053-2a95a90aa9ce	2024-01-17	Warnings	Exact identifier application number: M017
Green Guard Hydrocortisone 1%	HYDROCORTISONE	Unifirst First Aid Corporation	bd348e2a-57b1-3f17-e053-2a95a90a8bdc	2024-01-17	Warnings	Exact identifier application number: M017
Pain Relief	LIDOCAINE, MENTHOL	HUMN Pharmaceuticals Inc	6c96f94a-e724-eab3-e053-2991aa0aab88	2024-01-17	Warnings	Exact identifier application number: M017
CVS Health Lidocaine Pain Relief	LIDOCAINE	Natural Essentials, Inc.	52e82e70-53b7-4ecb-be39-fe10c94cc444	2024-01-17	Warnings	Exact identifier application number: M017
CVS Health XL Lidocaine Pain Relief	LIDOCAINE	NATURAL ESSENTIALS, INC.	ec16da91-8244-402b-b8d8-84896094ac2c	2024-01-17	Warnings	Exact identifier application number: M017
Anti-itch	DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE	Target Corporation	f444b0a6-2ed3-4236-8206-342150290675	2024-01-17	Warnings	Exact identifier application number: M017
Maximum Strength Hydrocortisone Anti-itch	HYDROCORTISONE 1%	Target Corporation	4ff39cb8-3a20-4fe7-9829-1e882a484668	2024-01-17	Warnings	Exact identifier application number: M017
Salonpas Pain Relieving LIDOCAINE 4% FLEX	LIDOCAINE	Hisamitsu Pharmaceutical Co., Inc.	9507f727-c49f-4de4-9d64-b6d977d568ab	2024-01-17	Warnings	Exact identifier application number: M017
Burn	LIDOCAINE HYDROCHLORIDE	Nantong Health & Beyond Hygienic Products Inc.	eca272cb-ac8f-982b-e053-2995a90aa8b2	2024-01-15	Warnings	Exact identifier application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
727161	menthol 8 % Topical Cream	PSN	547abe39-3af3-4d70-99dd-caf8d67feda2	26
727161	menthol 80 MG/ML Topical Cream	SCD	547abe39-3af3-4d70-99dd-caf8d67feda2	26
727161	menthol 8 % Topical Cream	SY	547abe39-3af3-4d70-99dd-caf8d67feda2	26

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
62212-252-03	62212025203	400 g in 1 BOTTLE (62212-252-03)	400 g	2013-01-01	No	No	Current