Frankincense and Myrrh Foot Pain Relief

Product NDC: 42346-302
11-digit product format: 423460302
Labeler code: 42346
Product ID: 42346-302_46e1e8df-9489-b1cc-e063-6394a90a1521
Type: HUMAN OTC DRUG
Nonproprietary name: Menthol
Dosage form: OIL
Route: TOPICAL
Labeler: WISE CONSUMER PRODUCTS CO.
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2024-02-14
Substance: MENTHOL
Active strength: 20 mg/mL
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: Frankincense and Myrrh Foot Pain Relief
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL	20 mg/mL

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
2675594	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
115f1abc-34aa-3c20-e063-6294a90a9764	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
42346-302-58	Frankincense and Myrrh Foot Pain Relief	59 mL in 1 BOTTLE, DROPPER	OIL	59		2
42346-302-58	Frankincense and Myrrh Foot Pain Relief	2 in 1 CARTON	OIL	2		2
42346-302-59	Frankincense and Myrrh Foot Pain Relief	59 mL in 1 BOTTLE, DROPPER	OIL	59		2
42346-302-59	Frankincense and Myrrh Foot Pain Relief	1 in 1 CARTON	OIL	1		2
42346-302-59	Frankincense and Myrrh Foot Pain Relief Combo Pack	1 in 1 CARTON	OIL		20 mg in 1mL	1
42346-302-59	Frankincense and Myrrh Foot Pain Relief Combo Pack	59 mL in 1 BOTTLE, DROPPER	OIL	59 mL	20 mg in 1mL	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
42346-302	FRANKINCENSE AND MYRRH FOOT PAIN RELIEF (MENTHOL) OIL [WISE CONSUMER PRODUCTS CO.]	1	Current NDC, 4 package rows	20240224_115f1abc-34aa-3c20-e063-6294a90a9764.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 106 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Pain Itch Relief	LIDOCAINE HCI	Trifecta Pharmaceutical USA LLC	f40b19a8-795c-f514-e053-2a95a90a6d15	2024-12-20	Warnings	Exact identifier application number: M017
Muscle Rub Cream	MENTHOL 10%, METHYL SALICYLATE 15%	Trifecta Pharmaceuticals USA, LLC.	44d3638d-f29b-0e01-e054-00144ff88e88	2024-12-20	Warnings	Exact identifier application number: M017
Rhuli Gel	CAMPHOR, MENTHOL	Trifecta Pharmaceuticals USA, LLC.	4fbb3c23-ed47-336e-e054-00144ff8d46c	2024-12-20	Warnings	Exact identifier application number: M017
Hydrocortisone Cream with Aloe	HYDROCORTISONE	Rugby Laboratories	132982ea-cce6-687c-e063-6294a90a4632	2024-12-20	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE 1%	Pharmacy Value Alliance LLC	9bb98452-a605-5c20-e053-2995a90a1ea7	2024-12-20	Warnings	Exact identifier application number: M017
DCH Cooling Pain Relief	MENTHOL 10.5%	Derma Care Research Labs, LLC	00dcdae0-c744-8402-e063-6294a90a12f8	2024-12-20	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE 1%	Pharmacy Value Alliance LLC	ab95e606-69f0-1d58-e053-2a95a90a073b	2024-12-20	Warnings	Exact identifier application number: M017
Itch Relief Cream	ZINC ACETATE 0.1%, DIPHENHYDRAMINE HYDROCHLORIDE 2%	Pharmacy Value Alliance LLC	37fe6d82-adee-4f58-e054-00144ff88e88	2024-12-20	Warnings	Exact identifier application number: M017
Warrior First Aid Anti Itch	DIPHENHYDRAMINE HCL 2%, ZINC ACETATE 0.1%	Derma Care Research Labs, LLC	ec6e9a5b-c61d-a385-e053-2995a90ac936	2024-12-20	Warnings	Exact identifier application number: M017
DCH Burn Relief	LIDOCAINE HCL	Derma Care Research Labs, LLC	ff227154-cf3b-9796-e053-6294a90a5535	2024-12-20	Warnings	Exact identifier application number: M017
Outback Pain Relief	CAMPHOR 6%, MENTHOL 16%	Derma Care Research Labs, LLC	c238c930-2012-2d48-e053-2a95a90a8a4a	2024-12-20	Warnings	Exact identifier application number: M017
Meijer Pain Relief	LIDOCAINE HCL 4%	Meijer	f31b11ed-2ff9-5cfc-e053-2a95a90af2ca	2024-12-20	Warnings	Exact identifier application number: M017
Meijer Pain Relief	MENTHOL 10.5%	Meijer	bed81975-bd63-cf5b-e053-2995a90ac5fa	2024-12-20	Warnings	Exact identifier application number: M017
Mirakel Pain and Itch Relief	BENZOCAINE 20%, RESORCINOL 3%	Sanvio, Inc.	ed34d728-0275-e209-e053-2995a90a93ff	2024-12-20	Warnings	Exact identifier application number: M017
Meijer Pain Relief	LIDOCAINE 4%	Meijer	bed67c31-c479-6f9b-e053-2a95a90a5516	2024-12-20	Warnings	Exact identifier application number: M017
Blue-Emu Ultra with Hemp Seed	TROLAMINE SALICYLATE	Kingsway Pharmaceuticals dba NFI, LLC	80a3cf99-16e8-412b-ab9f-3d9d5cbb7aa9	2024-12-20	Warnings	Exact identifier application number: M017
Epsom Salts	MAGNESIUM SULFATE	International Wholesale Inc.	e4d9bc32-ac85-349f-e053-2995a90a032f	2024-12-19	Warnings	Exact identifier application number: M017
Epsom Salts	MAGNESIUM SULFATE	International Wholesale Inc.	e5f3edc2-1b79-533a-e053-2a95a90ae9b6	2024-12-19	Warnings	Exact identifier application number: M017
Leader	LIDOCAINE HCL	Cardinal Health	cea6bd2d-a265-1209-e053-2995a90ab0a5	2024-12-19	Warnings	Exact identifier application number: M017
Rugby Anti-Itch	CAMPHOR, MENTHOL	RUGBY LABORATORIES	99d8ad9e-46ec-15fc-e053-2995a90a0d17	2024-12-19	Warnings	Exact identifier application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
2675594	menthol 2 % Topical Oil	PSN	115f1abc-34aa-3c20-e063-6294a90a9764	2
2675594	menthol 20 MG/ML Topical Oil	SCD	115f1abc-34aa-3c20-e063-6294a90a9764	2
2675594	menthol 2 % Topical Oil	SY	115f1abc-34aa-3c20-e063-6294a90a9764	2
2045268	menthol 1.3 % Topical Lotion	PSN	46e2c8b6-bd94-7100-e063-6294a90ac998	1
2675594	menthol 2 % Topical Oil	PSN	46e2c8b6-bd94-7100-e063-6294a90ac998	1
2045268	menthol 13 MG/ML Topical Lotion	SCD	46e2c8b6-bd94-7100-e063-6294a90ac998	1
2675594	menthol 20 MG/ML Topical Oil	SCD	46e2c8b6-bd94-7100-e063-6294a90ac998	1
2045268	menthol 1.3 % Topical Lotion	SY	46e2c8b6-bd94-7100-e063-6294a90ac998	1
2675594	menthol 2 % Topical Oil	SY	46e2c8b6-bd94-7100-e063-6294a90ac998	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Sample	Exclude flag	Status
42346-302-58	42346030258	2 BOTTLE, DROPPER in 1 CARTON (42346-302-58) / 59 mL in 1 BOTTLE, DROPPER	2024-02-14	No	No	Current
42346-302-59	42346030259	1 BOTTLE, DROPPER in 1 CARTON (42346-302-59) / 59 mL in 1 BOTTLE, DROPPER	2024-02-14	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Menthol - WISE CONSUMER PRODUCTS CO. \| Innovation Labs, Inc.	WISE CONSUMER PRODUCTS CO. \| Innovation Labs, Inc.	2025-12-26	HUMAN OTC DRUG LABEL	2
Frankincense & Myrrh Foot Pain Relief Combo Pack	WISE CONSUMER PRODUCTS CO. \| Innovation Labs, Inc.	2025-12-26	HUMAN OTC DRUG LABEL	1