Pain Relieving

Product NDC
61010-4403
11-digit product format
610104403
Labeler code
61010
Product ID
61010-4403_10aa8eb6-5d50-bea9-e063-6394a90a3623
Type
HUMAN OTC DRUG
Nonproprietary name
menthol
Dosage form
GEL
Route
TOPICAL
Labeler
Safetec of America, Inc.
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2019-11-01
Substance
MENTHOL
Active strength
4 g/100g
NDC exclude flag
No
Listing certified through
2027-12-31
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
Pain Relieving
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL4 g/100g

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
415974Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
52ebf64d-095f-467e-bf51-dd8d33b58c7dAvailable on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
61010-4403-12024-02-13C16284748780-11030e365-2c4c-111a-e063-dadaa90a10e261010-4403-1
61010-4403-12024-01-30C16284748780-11030e365-2c4c-111a-e063-dadaa90a10e261010-4403-1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61010-4403-1Pain Relieving113.4 g in 1 TUBEGEL113.42

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61010-4403PAIN RELIEVING (MENTHOL) GEL [SAFETEC OF AMERICA, INC.]2Current NDC, Legacy NDC, 1 package rows20240214_52ebf64d-095f-467e-bf51-dd8d33b58c7d.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 106 of 151 · 3,020 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
HydrocortisoneHYDROCORTISONE 1%Pharmacy Value Alliance LLCab95e606-69f0-1d58-e053-2a95a90a073b2024-12-20WarningsExact identifier
application number: M017
Itch Relief CreamZINC ACETATE 0.1%, DIPHENHYDRAMINE HYDROCHLORIDE 2%Pharmacy Value Alliance LLC37fe6d82-adee-4f58-e054-00144ff88e882024-12-20WarningsExact identifier
application number: M017
Warrior First Aid Anti ItchDIPHENHYDRAMINE HCL 2%, ZINC ACETATE 0.1%Derma Care Research Labs, LLCec6e9a5b-c61d-a385-e053-2995a90ac9362024-12-20WarningsExact identifier
application number: M017
DCH Burn ReliefLIDOCAINE HCLDerma Care Research Labs, LLCff227154-cf3b-9796-e053-6294a90a55352024-12-20WarningsExact identifier
application number: M017
Outback Pain ReliefCAMPHOR 6%, MENTHOL 16%Derma Care Research Labs, LLCc238c930-2012-2d48-e053-2a95a90a8a4a2024-12-20WarningsExact identifier
application number: M017
Meijer Pain ReliefLIDOCAINE HCL 4%Meijerf31b11ed-2ff9-5cfc-e053-2a95a90af2ca2024-12-20WarningsExact identifier
application number: M017
Meijer Pain ReliefMENTHOL 10.5%Meijerbed81975-bd63-cf5b-e053-2995a90ac5fa2024-12-20WarningsExact identifier
application number: M017
Mirakel Pain and Itch ReliefBENZOCAINE 20%, RESORCINOL 3%Sanvio, Inc.ed34d728-0275-e209-e053-2995a90a93ff2024-12-20WarningsExact identifier
application number: M017
Meijer Pain ReliefLIDOCAINE 4%Meijerbed67c31-c479-6f9b-e053-2a95a90a55162024-12-20WarningsExact identifier
application number: M017
Blue-Emu Ultra with Hemp SeedTROLAMINE SALICYLATEKingsway Pharmaceuticals dba NFI, LLC80a3cf99-16e8-412b-ab9f-3d9d5cbb7aa92024-12-20WarningsExact identifier
application number: M017
Epsom SaltsMAGNESIUM SULFATEInternational Wholesale Inc.e4d9bc32-ac85-349f-e053-2995a90a032f2024-12-19WarningsExact identifier
application number: M017
Epsom SaltsMAGNESIUM SULFATEInternational Wholesale Inc.e5f3edc2-1b79-533a-e053-2a95a90ae9b62024-12-19WarningsExact identifier
application number: M017
LeaderLIDOCAINE HCLCardinal Healthcea6bd2d-a265-1209-e053-2995a90ab0a52024-12-19WarningsExact identifier
application number: M017
Rugby Anti-ItchCAMPHOR, MENTHOLRUGBY LABORATORIES99d8ad9e-46ec-15fc-e053-2995a90a0d172024-12-19WarningsExact identifier
application number: M017
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

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
415974menthol 4 % Topical GelPSN52ebf64d-095f-467e-bf51-dd8d33b58c7d2
415974menthol 0.04 MG/MG Topical GelSCD52ebf64d-095f-467e-bf51-dd8d33b58c7d2
415974menthol 4 % Topical GelSY52ebf64d-095f-467e-bf51-dd8d33b58c7d2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
61010-4403-161010440301113.4 g in 1 TUBE (61010-4403-1) 113.4 g2019-11-010000-00-00NoNoCurrent