Thera Plus Extra Strength Muscle Rub Topical Analgesic

Product NDC
80684-139
11-digit product format
806840139
Labeler code
80684
Product ID
80684-139_3c1ad278-b7b9-7859-e063-6294a90a528a
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL
Dosage form
GEL
Route
TOPICAL
Labeler
FOURSTAR GROUP USA, INC.
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-03-03
Substance
MENTHOL
Active strength
25 mg/g
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
Thera Plus Extra Strength Muscle Rub Topical Analgesic
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL25 mg/g

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
282805Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
8a3b6adf-afbb-4d77-a19b-a6514ebd3b50Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80684-139-00Thera Plus Extra Strength Muscle Rub Topical Analgesic42.5 g in 1 TUBEGEL42.53

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80684-139THERA PLUS EXTRA STRENGTH MUSCLE RUB TOPICAL ANALGESIC (MENTHOL) GEL [FOURSTAR GROUP USA, INC.]2Current NDC, 1 package rows20250306_8a3b6adf-afbb-4d77-a19b-a6514ebd3b50.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 107 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
DCH Calaspray Itch ReliefPRAMOXINE HCL 1%, ZINC ACETATE 0.1%Derma Care Research Labs, LLCfda2afaf-3cd0-92b3-e053-6394a90a74932024-12-19WarningsExact identifier
application number: M017
DCH Nerve Pain Relief Roll-OnLIDOCAINE HCL 4%, MENTHOL 1%Derma Care Research Labs, LLCff32cbb2-79eb-9158-e053-6394a90ac3572024-12-19WarningsExact identifier
application number: M017
DCH Burn ReliefLIDOCAINE, 0.5%Derma Care Research Labsffd7be08-0510-dfcb-e053-6394a90ad2862024-12-19WarningsExact identifier
application number: M017
DCH Arthritis Pain Relief Roll-OnCAPSAISIN 0.1%Derma Care Research Labs, LLCfda0d359-95eb-8b38-e053-6294a90a7b882024-12-19WarningsExact identifier
application number: M017
DCH Pain RelievingMENTHOL 2%Derma Care Research Labs, LLCff49ee63-6a87-c7a7-e053-6294a90a77a32024-12-19WarningsExact identifier
application number: M017
Warrior Pain Relief Roll-On Maximum StrengthLIDOCAINE HCL 4%Derma Care Research Labs, LLCdd80e560-6467-2166-e053-2995a90a88a82024-12-19WarningsExact identifier
application number: M017
DCH Labs Cool and Heat Roll-OnMENTHOL 16%Derma Care Research Labs, LLCd35d7720-44ce-3624-e053-2995a90a7fb42024-12-19WarningsExact identifier
application number: M017
Dr Goldsons PainMENTHOL 8%, METHYL SALICYLATE 30%Derma Care Research Labs, LLCfb34b0d3-ccc0-305e-e053-6394a90a231d2024-12-19WarningsExact identifier
application number: M017
Warrior Pain RelievingCAMPHOR 4%, MENTHOL 10%, METHYL SALICYLATE 30%Derma Care Research Labs, LLCdd06af3c-5452-9759-e053-2a95a90afc212024-12-19WarningsExact identifier
application number: M017
Warrior Burn Relief Aloe Maximum StrengthLIDOCAINE HCL 4%Derma Care Research Labs, LLCec6efa4b-dcbe-1c2b-e053-2995a90ae0432024-12-19WarningsExact identifier
application number: M017
DCH Arthritis ReliefTROLAMIN SALICYLATE 10%Derma Care Research Labs, LLCff31e515-5780-b77d-e053-6394a90af6b92024-12-19WarningsExact identifier
application number: M017
DCH Pain ReliefLIDOCAINE 4%Derma Care Research Labs, LLC00efda74-d434-04be-e063-6294a90a6d982024-12-19WarningsExact identifier
application number: M017
Dollar General Cold Therapy Pain ReliefMENTHOL 5%Dolgencorp, LLCff3284d1-e73c-93bf-e053-6294a90aaf4e2024-12-19WarningsExact identifier
application number: M017
Dollar General Pain Relieving Patch with LidocaineLIDOCAINEDOLGENCORP, LLC55828cd1-3a1e-48ac-bb01-4c50b96d09a22024-12-19WarningsExact identifier
application number: M017
DCH Nerve Pain ReliefLIDOCAINE 4%, MENTHOL 1%Derma Care Research Labs, LLC00db480a-e510-a64d-e063-6394a90a46952024-12-19WarningsExact identifier
application number: M017
Pain, Burn, and Itch ReliefBENZOCAINE 20%, MENTHOL 0.5%Derma Care Research Labs, LLCfd9fe09f-3ae9-c5f5-e053-6394a90ad6912024-12-19WarningsExact identifier
application number: M017
DCH Cooling Pain ReliefMENTHOL 4%Derma Care Research Labs, LLC00ed3175-c3ba-6545-e063-6394a90acfd12024-12-19WarningsExact identifier
application number: M017
DCH Pain ReliefLIDOCAINE HCL 4%Derma Care Research Labs, LLC00dd70f3-ecc3-33ba-e063-6294a90a4f322024-12-19WarningsExact identifier
application number: M017
Walgreens Kinesiology Pain ReliefLIDOCAINE, MENTHOLWalgreen Co.0fdbb310-8e65-4e0c-b413-a093964324a22024-12-19WarningsExact identifier
application number: M017
Signature Care Medicated Cold and Hot PatchMENTHOLSafeway0335f1b3-5c8a-67b8-e063-6294a90a98472024-12-19WarningsExact identifier
application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
282805menthol 2.5 % Topical GelPSN8a3b6adf-afbb-4d77-a19b-a6514ebd3b503
282805menthol 0.025 MG/MG Topical GelSCD8a3b6adf-afbb-4d77-a19b-a6514ebd3b503
282805menthol 2.5 % Topical GelSY8a3b6adf-afbb-4d77-a19b-a6514ebd3b503

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
80684-139-008068401390042.5 g in 1 TUBE (80684-139-00) 42.5 g2025-03-03NoNoCurrent