TopCare Maximum Strength Pain Relieving

Product NDC
36800-894
11-digit product format
368000894
Labeler code
36800
Product ID
36800-894_139ed16f-1958-417e-bf0e-4fe6f6f4ffaa
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL, UNSPECIFIED FORM
Dosage form
LIQUID
Route
TOPICAL
Labeler
Topco Associates LLC
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-03-25
Substance
MENTHOL, UNSPECIFIED FORM
Active strength
160 mg/mL
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
TopCare Maximum Strength Pain Relieving
Brand name suffix
Analgesic
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL, UNSPECIFIED FORM160 mg/mL

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
866084Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
dc80d2f9-e3eb-4feb-bad5-7d6ab107f9abAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
473d070d-1c38-488e-b991-c4d1bf45aab8Product name120210201

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
36800-894-01TopCare Maximum Strength Pain RelievingAnalgesic1 in 1 CARTONLIQUID15
36800-894-01TopCare Maximum Strength Pain RelievingAnalgesic74 mL in 1 BOTTLE, WITH APPLICATORLIQUID745

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
36800-894TOPCARE MAXIMUM STRENGTH PAIN RELIEVING ANALGESIC (MENTHOL, UNSPECIFIED FORM) LIQUID [TOPCO ASSOCIATES LLC]4Current NDC, Legacy NDC, 2 package rows20241107_dc80d2f9-e3eb-4feb-bad5-7d6ab107f9ab.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
866084menthol 16 % Topical SolutionPSNdc80d2f9-e3eb-4feb-bad5-7d6ab107f9ab5
866084menthol 160 MG/ML Topical SolutionSCDdc80d2f9-e3eb-4feb-bad5-7d6ab107f9ab5
866084menthol 16 % Topical SolutionSYdc80d2f9-e3eb-4feb-bad5-7d6ab107f9ab5

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
36800-894-01368000894011 BOTTLE, WITH APPLICATOR in 1 CARTON (36800-894-01) / 74 mL in 1 BOTTLE, WITH APPLICATOR2020-03-250000-00-00NoNoCurrent