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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UNII Substances#

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openFDA label cross-check#

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ActivICEMENTHOLMedline Industries, LP834adeb9-38ad-0cfe-e053-2991aa0af82f2025-10-23WarningsExact identifier
rxcui: 2119857

DailyMed RxNorm Mappings#

Set ID, RxNorm string, TTY table
Set IDRxNorm stringTTYSPL versionLabelEffective
834adeb9-38ad-0cfe-e053-2991aa0af82fmenthol 0.08 MG/MG Topical Gel [ActivICE]SBD11984 ActivIce gel20251023
834adeb9-38ad-0cfe-e053-2991aa0af82fActivICE 8 % Topical GelPSN11984 ActivIce gel20251023
834adeb9-38ad-0cfe-e053-2991aa0af82fActivICE 0.08 MG/MG Topical GelSY11984 ActivIce gel20251023
9d0012ed-a50a-a936-e053-2995a90a6100menthol 0.08 MG/MG Topical Gel [ActivICE]SBD1These 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
9d0012ed-a50a-a936-e053-2995a90a6100ActivICE 0.08 MG/MG Topical GelSY1These 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
9d0012ed-a50a-a936-e053-2995a90a6100ActivICE 8 % Topical GelPSN1These 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