FDA.reportPublic FDA data

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
IngredientStrength
MENTHOL20 mg/mL

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
2675594Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
115f1abc-34aa-3c20-e063-6294a90a9764Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42346-302-58Frankincense and Myrrh Foot Pain Relief59 mL in 1 BOTTLE, DROPPEROIL592
42346-302-58Frankincense and Myrrh Foot Pain Relief2 in 1 CARTONOIL22
42346-302-59Frankincense and Myrrh Foot Pain Relief59 mL in 1 BOTTLE, DROPPEROIL592
42346-302-59Frankincense and Myrrh Foot Pain Relief1 in 1 CARTONOIL12
42346-302-59Frankincense and Myrrh Foot Pain Relief Combo Pack1 in 1 CARTONOIL20 mg in 1mL1
42346-302-59Frankincense and Myrrh Foot Pain Relief Combo Pack59 mL in 1 BOTTLE, DROPPEROIL59 mL20 mg in 1mL1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
42346-302FRANKINCENSE AND MYRRH FOOT PAIN RELIEF (MENTHOL) OIL [WISE CONSUMER PRODUCTS CO.]1Current NDC, 4 package rows20240224_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 120 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Alocane MaxLIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDEQuest Products LLC0a35ac19-6883-a733-e063-6294a90ad22d2024-11-05WarningsExact identifier
application number: M017
Alocane PlusLIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDEQuest Products, Inc.cfe8114b-df65-064b-e053-2a95a90a33f62024-11-05WarningsExact identifier
application number: M017
Alocane BotanicalsLIDOCAINE HYDROCHLORIDEQuest Products, LLC.02a8e5c7-56f4-eb0d-e063-6294a90a80cd2024-11-05WarningsExact identifier
application number: M017
Alocane Emergency Burn PadsLIDOCAINE HYDROCHLORIDEQuest Products, Inc.fe58bb89-7216-4121-afd3-d1438bdfbfa22024-11-05WarningsExact identifier
application number: M017
Licefreee AfterLicePRAMOXINE HCITec Laboratories Inc.06c4cc42-a215-3949-e063-6394a90a665e2024-11-05WarningsExact identifier
application number: M017
Antibacterial Lidocaine Wound GelBENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDEASO LLCcb9505b7-222d-3a24-e053-2a95a90a0b642024-11-05WarningsExact identifier
application number: M017
TopCare Pain Relieving AnalgesicLIDOCAINE HYDROCHLORIDETopco Associates LLC6b4783e0-1987-4838-9e8c-b95426d62b282024-11-05WarningsExact identifier
application number: M017
Eagle Green BalmCAMPHOR MENTHOLBorden Company (Private) Limited6f7a796b-a31c-0e60-e053-2a91aa0a022b2024-11-04WarningsExact identifier
application number: M017
Muscular BalmCAPSAICIN MENTHOL METHYL SALICYLATEBorden Company (Private) Limiteded79f14e-6b3d-4bf2-9c34-d019c1ba25822024-11-04WarningsExact identifier
application number: M017
Hydrocortisone with AloeHYDROCORTISONEA-S Medication Solutions3e0aed2b-fee1-4a0c-a3d2-72cd2b3008e32024-11-04WarningsExact identifier
application number: M017
Walgreens Ice Blue Pain Relieving Topical AnalgesicMENTHOL, UNSPECIFIED FORMWalgreen Company1c0ee442-ffd2-4f6c-aab2-f70e295378ad2024-11-04WarningsExact identifier
application number: M017
Walgreen Cool n Heat Maximum Strength Pain RelievingMENTHOL, UNSPECIFIED FORMWalgreen Companyd5c79476-dde8-4a85-8878-bc2ac3a3d70b2024-11-04WarningsExact identifier
application number: M017
LIDOCAINELIDOCAINESTRATUS PHARMACEUTICALS INC87a4f559-a4f6-4b9f-98de-b55b073a11c62024-11-01WarningsExact identifier
application number: M017
Walgreens Nerve Pain Relieving Topical AnalgesicLIDOCAINE HYDROCHLORIDE AND MENTHOL, UNSPECIFIED FORMWalgreen Company83849eca-e02f-4b43-b3a7-b25e987e08a82024-10-31WarningsExact identifier
application number: M017
Sanar Naturals Arnica WhiteCAMPHORSanvall Enterprises, Inc192039a2-aed6-821b-e063-6394a90a7f292024-10-31WarningsExact identifier
application number: M017
Sanar Naturals Arnica ReforzadaCAMPHORSanvall Enterprises, Inc1921a4b1-cd36-195e-e063-6294a90a87932024-10-31WarningsExact identifier
application number: M017
Sanar Naturals Arnica Pain Releiving Roll On with CamphorCAMPHORSanvall Enterprises, Inc173db0e2-611f-55b9-e063-6394a90ac9872024-10-31WarningsExact identifier
application number: M017
Sanar Naturals CamphorCAMPHORSanvall Enterprises, Inc1921e851-cf83-0bdb-e063-6294a90a357f2024-10-31WarningsExact identifier
application number: M017
cortisoneHYDROCORTISONECVS Pharmacyc766deac-d993-4e48-a5c3-4cfde7338dff2024-10-31WarningsExact identifier
application number: M017
Walgreens Pain Relieving with Lavender AnalgesicLIDOCAINE HYDROCHLORIDEWalgreen Company6c7b39c8-5b65-430a-a529-5b6b14adce182024-10-31WarningsExact identifier
application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
2675594menthol 2 % Topical OilPSN115f1abc-34aa-3c20-e063-6294a90a97642
2675594menthol 20 MG/ML Topical OilSCD115f1abc-34aa-3c20-e063-6294a90a97642
2675594menthol 2 % Topical OilSY115f1abc-34aa-3c20-e063-6294a90a97642
2045268menthol 1.3 % Topical LotionPSN46e2c8b6-bd94-7100-e063-6294a90ac9981
2675594menthol 2 % Topical OilPSN46e2c8b6-bd94-7100-e063-6294a90ac9981
2045268menthol 13 MG/ML Topical LotionSCD46e2c8b6-bd94-7100-e063-6294a90ac9981
2675594menthol 20 MG/ML Topical OilSCD46e2c8b6-bd94-7100-e063-6294a90ac9981
2045268menthol 1.3 % Topical LotionSY46e2c8b6-bd94-7100-e063-6294a90ac9981
2675594menthol 2 % Topical OilSY46e2c8b6-bd94-7100-e063-6294a90ac9981

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
42346-302-58423460302582 BOTTLE, DROPPER in 1 CARTON (42346-302-58) / 59 mL in 1 BOTTLE, DROPPER2024-02-14NoNoCurrent
42346-302-59423460302591 BOTTLE, DROPPER in 1 CARTON (42346-302-59) / 59 mL in 1 BOTTLE, DROPPER2024-02-14NoNoCurrent