Thunder Fck Male Genital Desensitizer

Product NDC
70742-587
11-digit product format
707420587
Labeler code
70742
Product ID
70742-587_2fab552b-5495-e52c-e063-6394a90a8fea
Type
HUMAN OTC DRUG
Nonproprietary name
BENZOCAINE
Dosage form
LIQUID
Route
TOPICAL
Labeler
PRODUCT MAX GROUP INC
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-02-13
Substance
BENZOCAINE
Active strength
75 mg/mL
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
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
Thunder Fck Male Genital Desensitizer
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZOCAINE75 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
U3RSY48JW5Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
93188a42-0d3c-4159-bdc7-bbc5ec5c6744Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70742-587-00Thunder Fck Male Genital Desensitizer30 mL in 1 BOTTLELIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70742-587THUNDER FCK MALE GENITAL DESENSITIZER (BENZOCAINE) LIQUID [PRODUCT MAX GROUP INC]1Current NDC, 1 package rows20250309_93188a42-0d3c-4159-bdc7-bbc5ec5c6744.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 113 of 151 · 3,020 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
VAGISIL Anti-Itch Medicated Wipes Maximum StrengthPRAMOXINE HYDROCHLORIDECombe Incorporatedb848f53d-8aea-4efe-aa2c-009d5121fc332024-12-12WarningsExact identifier
application number: M017
Walgreens Cool and HeatMENTHOL 16%Walgreensce1585f4-ca65-8d0c-e053-2995a90a8e892024-12-11WarningsExact identifier
application number: M017
Walgreens Cool n HeatLIDOCAINE 4%Walgreensce1b21d6-7aa6-2b18-e053-2995a90a4c912024-12-11WarningsExact identifier
application number: M017
Walgreens Pain Burn Itch ReliefBENZOCAINE 20%, MENTHOL 0.5%Walgreenscc6e4b42-fdd8-6ff7-e053-2995a90a3d1d2024-12-11WarningsExact identifier
application number: M017
Pramoxine Itch reliefPRAMOXINE HCL 1%CVSe947694c-c122-0291-e053-2995a90ac39a2024-12-11WarningsExact identifier
application number: M017
Arthritis CreamTROLAMINE SALICYLATE 10%CVSd1663f50-479b-4d55-e053-2995a90a223f2024-12-11WarningsExact identifier
application number: M017
CVS Pain ReliefMENTHOL 4%CVSd1660d55-1ee0-7aa2-e053-2995a90a65792024-12-11WarningsExact identifier
application number: M017
CVS Muscle RubMENTHOL 10%, METHYL SALICYLATE 15%CVS Healthc72c9a95-4226-6d69-e053-2a95a90a8e1c2024-12-11WarningsExact identifier
application number: M017
BENGAY ULTRA STRENGTH NON-GREASYCAMPHOR (SYNTHETIC), MENTHOL, UNSPECIFIED FORM, AND METHYL SALICYLATEKenvue Brands LLC0a41ec65-bd0b-4fc6-807d-74f353341cc72024-12-11WarningsExact identifier
application number: M017
Serum XLIDOCAINE HYDROCHLORIDEAO Biologix, LLCe07b6268-6400-6849-e053-2a95a90a8b3e2024-12-11WarningsExact identifier
application number: M017
PlusCBD Pain Cream (Penetrating) 2ozCAMPHOR, MENTHOLCV Sciences, Inc.ca39d327-6bf3-3408-e053-2a95a90af2d52024-12-11WarningsExact identifier
application number: M017
Blistex MedicatedDIMETHICONE, CAMPHOR (SYNTHETIC), MENTHOL, AND PHENOLBlistex Inc.e95439d3-f12b-4c1c-999a-79f2ddba4cfb2024-12-11WarningsExact identifier
application number: M017
Blistex Foille Medicated First AidBENZOCAINE AND CHLOROXYLENOLBlistex Inc.e2eca808-e97b-43e0-aa51-7025cc61c7a82024-12-11WarningsExact identifier
application number: M017
HydrocortisoneHYDROCORTISONEJ&A Digital Inc.ff95a536-35b3-4006-b43c-cce359e86aa92024-12-10WarningsExact identifier
application number: M017
Methyl SalicylateMETHYL SALICYLATEAlexso, Inceef555d3-f23d-4847-93f3-fa7a06072a0f2024-12-09WarningsExact identifier
application number: M017
Lidocaine 4 PercentLIDOCAINESA3, LLC651710db-3c50-4bcf-b7cc-9ed24f6634272024-12-09WarningsExact identifier
application number: M017
HealthWise Pain Relief Lidocaine PatchLIDOCAINE 4%Veridian Healthcare28db1c03-d01f-83ea-e063-6294a90aee262024-12-09WarningsExact identifier
application number: M017
Joint and Muscle Pain ReliefMENTHOLAllure Labse82f99fd-c2ef-686f-e053-2a95a90a1dc92024-12-09WarningsExact identifier
application number: M017
Tough Love Pain RelievingLIDOCAINE HCLAllure Labsee8c1a2b-36ef-6fd7-e053-2a95a90a9c012024-12-09WarningsExact identifier
application number: M017
CapsaicinCAPSAICINSA3, LLC5617e91d-e650-4a0d-8565-b8288ea41c772024-12-09WarningsExact identifier
application number: M017

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
70742-587-007074205870030 mL in 1 BOTTLE (70742-587-00) 30 ml2025-02-13NoNoCurrent