Bengay Zero Degrees Menthol Pain Relieving

Product NDC
58232-4036
11-digit product format
582324036
Labeler code
58232
Product ID
58232-4036_4ad4eef9-f79b-4de2-baf9-d5a083a6a552
Type
HUMAN OTC DRUG
Nonproprietary name
Menthol
Dosage form
GEL
Route
TOPICAL
Labeler
Johnson & Johnson Consumer Inc.
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2011-09-15
Marketing end
0000-00-00
Substance
MENTHOL, UNSPECIFIED FORM
Active strength
50 mg/g
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

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 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct58232-4036DDiscontinued by firm2026-09-14
excluded packagepackage58232-403658232-4036-1DDiscontinued by firm2026-09-14

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 · 24 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage58232-4036-1d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage58232-4036-1f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31excluded productproduct2ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-31excluded packagepackage58232-4036-12ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28excluded productproducta1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-28excluded packagepackage58232-4036-1a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21excluded productproductcfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-21excluded packagepackage58232-4036-1cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10excluded productproductcdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-10excluded packagepackage58232-4036-1cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31excluded productproduct302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-31excluded packagepackage58232-4036-1302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20excluded productproducted331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-20excluded packagepackage58232-4036-1ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10excluded productproduct0efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-10excluded packagepackage58232-4036-10efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08excluded productproductad56d346431e…cc804d4bbf1e…
2024-11-09 02:27 UTC · source 2024-11-08excluded packagepackage58232-4036-1ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03excluded productproduct367a005e9d99…383a685ebd0f…
2024-10-04 04:10 UTC · source 2024-10-03excluded packagepackage58232-4036-1367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09excluded productproduct557ba5c1ecfa…9c80585c8c6e…
2024-07-10 04:00 UTC · source 2024-07-09excluded packagepackage58232-4036-1557ba5c1ecfa…9c80585c8c6e…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
MentholACTIVE INGREDIENTL7T10EIP3ABENGAY ZERO DEGREES MENTHOL PAIN RELIEVING (MENTHOL) CREAM [JOHNSON & JOHNSON CONSUMER PRODUCTS COMPANY, DIVISION OF JOHNSON & JOHNSON CONSUMER COMPANIES, INC.]1
MentholACTIVE MOIETYL7T10EIP3ABENGAY ZERO DEGREES MENTHOL PAIN RELIEVING (MENTHOL) CREAM [JOHNSON & JOHNSON CONSUMER PRODUCTS COMPANY, DIVISION OF JOHNSON & JOHNSON CONSUMER COMPANIES, INC.]1
AlcoholINACTIVE INGREDIENT3K9958V90MBENGAY ZERO DEGREES MENTHOL PAIN RELIEVING (MENTHOL) CREAM [JOHNSON & JOHNSON CONSUMER PRODUCTS COMPANY, DIVISION OF JOHNSON & JOHNSON CONSUMER COMPANIES, INC.]1
AminomethylpropanolINACTIVE INGREDIENTLU49E6626QBENGAY ZERO DEGREES MENTHOL PAIN RELIEVING (MENTHOL) CREAM [JOHNSON & JOHNSON CONSUMER PRODUCTS COMPANY, DIVISION OF JOHNSON & JOHNSON CONSUMER COMPANIES, INC.]1
Camphor (Synthetic)INACTIVE INGREDIENT5TJD82A1ETBENGAY ZERO DEGREES MENTHOL PAIN RELIEVING (MENTHOL) CREAM [JOHNSON & JOHNSON CONSUMER PRODUCTS COMPANY, DIVISION OF JOHNSON & JOHNSON CONSUMER COMPANIES, INC.]1
Ethylhexyl IsononanoateINACTIVE INGREDIENTI6KB4GE3K4BENGAY ZERO DEGREES MENTHOL PAIN RELIEVING (MENTHOL) CREAM [JOHNSON & JOHNSON CONSUMER PRODUCTS COMPANY, DIVISION OF JOHNSON & JOHNSON CONSUMER COMPANIES, INC.]1
FD&C Blue No. 1INACTIVE INGREDIENTH3R47K3TBDBENGAY ZERO DEGREES MENTHOL PAIN RELIEVING (MENTHOL) CREAM [JOHNSON & JOHNSON CONSUMER PRODUCTS COMPANY, DIVISION OF JOHNSON & JOHNSON CONSUMER COMPANIES, INC.]1
GlycerinINACTIVE INGREDIENTPDC6A3C0OXBENGAY ZERO DEGREES MENTHOL PAIN RELIEVING (MENTHOL) CREAM [JOHNSON & JOHNSON CONSUMER PRODUCTS COMPANY, DIVISION OF JOHNSON & JOHNSON CONSUMER COMPANIES, INC.]1
Isopropyl AlcoholINACTIVE INGREDIENTND2M416302BENGAY ZERO DEGREES MENTHOL PAIN RELIEVING (MENTHOL) CREAM [JOHNSON & JOHNSON CONSUMER PRODUCTS COMPANY, DIVISION OF JOHNSON & JOHNSON CONSUMER COMPANIES, INC.]1
Polysorbate 60INACTIVE INGREDIENTCAL22UVI4MBENGAY ZERO DEGREES MENTHOL PAIN RELIEVING (MENTHOL) CREAM [JOHNSON & JOHNSON CONSUMER PRODUCTS COMPANY, DIVISION OF JOHNSON & JOHNSON CONSUMER COMPANIES, INC.]1
Propylene GlycolINACTIVE INGREDIENT6DC9Q167V3BENGAY ZERO DEGREES MENTHOL PAIN RELIEVING (MENTHOL) CREAM [JOHNSON & JOHNSON CONSUMER PRODUCTS COMPANY, DIVISION OF JOHNSON & JOHNSON CONSUMER COMPANIES, INC.]1
WaterINACTIVE INGREDIENT059QF0KO0RBENGAY ZERO DEGREES MENTHOL PAIN RELIEVING (MENTHOL) CREAM [JOHNSON & JOHNSON CONSUMER PRODUCTS COMPANY, DIVISION OF JOHNSON & JOHNSON CONSUMER COMPANIES, INC.]1