FDA.reportPublic FDA data

MENTHOL, CAMPHOR

Product NDC
72937-006
11-digit product format
729370006
Labeler code
72937
Product ID
72937-006_44130c5e-f752-2432-e063-6394a90aa5ec
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL, CAMPHOR
Dosage form
GEL
Route
TOPICAL
Labeler
SUNSET NOVELTIES, INC
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-09-22
Marketing end
2027-01-03
Substance
MENTHOL; CAMPHOR, (-)-
Active strength
6; 2 g/100g; g/100g
NDC exclude flag
No
Current FDA listing
Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 8 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct72937-006DDiscontinued by firm2026-10-20
excluded productproduct72937-006DDiscontinued by firm2026-10-20
excluded packagepackage72937-00672937-006-02DDiscontinued by firm2026-10-20
excluded packagepackage72937-00672937-006-04DDiscontinued by firm2026-10-20
excluded packagepackage72937-00672937-006-16DDiscontinued by firm2026-10-20
excluded packagepackage72937-00672937-006-40DDiscontinued by firm2026-10-20
excluded packagepackage72937-00672937-006-80DDiscontinued by firm2026-10-20
excluded packagepackage72937-00672937-006-42DDiscontinued by firm2026-10-20

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 6 matching rows.

View current auxiliary records. · View the auxiliary file history.

Dataset, Scope, Package NDC table
DatasetScopePackage NDC
excluded productproduct
excluded packagepackage72937-006-04
excluded packagepackage72937-006-80
excluded packagepackage72937-006-40
excluded packagepackage72937-006-16
excluded packagepackage72937-006-02

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, CAMPHOR

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL6 g/100g
CAMPHOR, (-)-2 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
L7T10EIP3AInternal UNII lookup
213N3S8275Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
f03090fa-f7e6-f53a-e053-2a95a90aa819Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
4d7a96d5-8256-4268-9a6c-25ea66d321feProduct name120180814
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72937-006-02MENTHOL, CAMPHOR59 g in 1 BOTTLEGEL596
72937-006-04MENTHOL, CAMPHOR118 g in 1 BOTTLEGEL1186
72937-006-08MENTHOL, CAMPHOR236 g in 1 BOTTLEGEL2366
72937-006-16MENTHOL, CAMPHOR472 g in 1 BOTTLEGEL4726

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72937-006MENTHOL, CAMPHOR GEL [SUNSET NOVELTIES, INC]5Current NDC, Legacy NDC, 4 package rows20241121_f03090fa-f7e6-f53a-e053-2a95a90aa819.zip
72937-006MENTHOL, CAMPHOR GEL [SUNSET NOVELTIES, INC]3Current NDC, Legacy NDC20240207_fc9d43a3-d59d-0ee5-e053-6294a90a4539.zip
72937-006MENTHOL, CAMPHOR GEL [SUNSET NOVELTIES, INC]1Current NDC, Legacy NDC20240209_10d0a0ac-aaad-7750-e063-6294a90a30fd.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 23 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Kevo-ProphenJUNIPER TARFaeve, LLC4fe773a8-77cd-831e-e063-6294a90ae2ca2026-04-20WarningsExact identifier
application number: M017
BeeVenomMETHYL SALICYLATEMenper Distributors, Inc.4fe7a986-336d-ad4e-e063-6294a90a0b8a2026-04-20WarningsExact identifier
application number: M017
BenzodentBENZOCAINEFocus Consumer Healthcare, LLC5fdcb871-d387-6352-e053-2991aa0a09da2026-04-20WarningsExact identifier
application number: M017
Tecnu CalagelDIPHENHYDRAMINE HYDROCHLORIDETec Laboratories Inc.8bc9cbfe-1dd4-18ed-e053-2a95a90a79662026-04-20WarningsExact identifier
application number: M017
Aemerry Numbing CreamMENTHOL 5%Da Capo Prima LLC4fefddaf-19c8-86b4-e063-6294a90abffc2026-04-20WarningsExact identifier
application number: M017
Sting Relief SwabBENZOCAINE4 Visions LLC4fc7a356-2f1d-85af-e063-6394a90aec6b2026-04-18WarningsExact identifier
application number: M017
Equate Lidocaine and Menthol Paraben FreeLIDOCAINE 4% PLUS MENTHOL 1%Walmart Stores Inc4fa917de-bc46-0b8d-e063-6294a90a218a2026-04-17WarningsExact identifier
application number: M017
LidoProLIDOCAINE AND MENTHOLAdvanced Rx of Tennessee, LLC4faa515f-6040-d948-e063-6294a90a187f2026-04-17WarningsExact identifier
application number: M017
Coleman Bite and Sting ReliefEXTERNAL ANESTHETIC AND FIRST AID ANTISEPTICWisconsin Pharmacal Company4fadf1f1-478a-5104-e063-6294a90a10cb2026-04-17WarningsExact identifier
application number: M017
Ice Gel ICE COLD ANALGESICMENTHOLUniversal Distribution Center LLC4f921ced-7722-cba5-e063-6294a90a650b2026-04-16WarningsExact identifier
application number: M017
Walgreens Capsaicin Hot PatchCAPSAICINWalgreen Co.41e959d8-f6ac-f5b4-e063-6294a90abd962026-04-16WarningsExact identifier
application number: M017
Walgreens Cold Therapy Pain Relieving PatchMENTHOLWalgreen Co.41e7574a-348f-8eb8-e063-6294a90a6e902026-04-16WarningsExact identifier
application number: M017
Coleman Sting and Bite ReliefEXTERNAL ANALGESIC AND FIRST AID ANTISEPTICWisconsin Pharmacal Company4f94ab35-3099-716c-e063-6294a90a8bea2026-04-16WarningsExact identifier
application number: M017
Kroger Witch HazelWITCH HAZELKroger Co.461407d0-fbf6-47e9-e063-6394a90a9a832026-04-16WarningsExact identifier
application number: M017
Stopain Extra Strength GelMENTHOLTroy Manufacturing, Inc.86fe4e8c-5279-445a-a19a-e694eac785fd2026-04-16WarningsExact identifier
application number: M017
Stopain ClinicalMENTHOL, UNSPECIFIED FORMTroy Manufacturing, Inc.4503208f-2808-4727-8066-c431230bd70b2026-04-16WarningsExact identifier
application number: M017
EXTRA STRENGTH STOPAIN COLD PAIN RELIEVING ROLL ONMENTHOLTROY MANUFACTURING, INC895896dc-0762-40a7-8313-cca10ce689842026-04-16WarningsExact identifier
application number: M017
HealthWise Medicated Cold Hot 5%MENTHOLVeridian Healthcare4f9b1b2d-1acc-e0a7-e063-6394a90aadbc2026-04-16WarningsExact identifier
application number: M017
Lidoease 2%LIDOCAINE HCL 2%PureTek Corporation3ba0c0ff-0f7a-7a29-e063-6294a90a547a2026-04-16WarningsExact identifier
application number: M017
Walgreens Lidocaine Pain Relieving Patch AssortedLIDOCAINEWalgreen Co.41e98f15-669f-4543-e063-6294a90a1ef72026-04-15WarningsExact identifier
application number: M017

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
72937-006-027293700060259 g in 1 BOTTLE (72937-006-02) 59 g2022-09-080000-00-00NoNoCurrent
72937-006-0472937000604118 g in 1 BOTTLE (72937-006-04) 118 g2022-09-080000-00-00NoNoCurrent
72937-006-0872937000608236 g in 1 BOTTLE (72937-006-08) 236 g2022-09-082027-01-03NoNoCurrent
72937-006-1672937000616472 g in 1 BOTTLE (72937-006-16) 472 g2022-09-080000-00-00NoNoCurrent