FDA.reportPublic FDA data

menthol 0.08 MG/MG Topical Gel [ActivICE]

RxCUI
2119857
RxNorm name
menthol 0.08 MG/MG Topical Gel [ActivICE]
Display name
menthol 0.08 MG/MG Topical Gel [ActivICE]
Full name
menthol 0.08 MG/MG Topical Gel [ActivICE]
Term type
SBD
Status
DailyMed mapping
Updated
2026-06-04 23:39:06

RxNav Current And Historical NDCs#

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No records found.

UNII Substances#

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No records found.

openFDA label cross-check#

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Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ActivICEMENTHOLMedline Industries, LP834adeb9-38ad-0cfe-e053-2991aa0af82f2026-09-01WarningsExact identifier
rxcui: 2119857

Reported adverse events (FAERS/openFDA)#

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

DailyMed RxNorm Mappings#

unique DailyMed labels mapped to this RxNorm concept page 1 of 1 · 2 matching rows.

Set ID, RxNorm mappings, Terms table
Set IDRxNorm mappingsTermsSPL versionLabelEffective
834adeb9-38ad-0cfe-e053-2991aa0af82fActivICE 8 % Topical Gel [PSN] · menthol 0.08 MG/MG Topical Gel [ActivICE] [SBD] · ActivICE 0.08 MG/MG Topical Gel [SY]311984 ActivIce gel20251023
9d0012ed-a50a-a936-e053-2995a90a6100ActivICE 8 % Topical Gel [PSN] · menthol 0.08 MG/MG Topical Gel [ActivICE] [SBD] · ActivICE 0.08 MG/MG Topical Gel [SY]31These highlights do not include all the information needed to use Diclofenac Sodium Topical Solution safely and effectively. See full prescribing information for Diclofenac Sodium Topical Solution.DICLOFENAC Sodium Topical Solution 1.5% w/w is for topical use only. Initial U.S. Approval: 198820200125