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 116 of 151 · 3,020 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Hempvana Cold As Ice Pain Relief Gel-PatchMENTHOLTelebrands Corp976a1bb2-b776-8199-e053-2995a90a1a1b2024-11-20WarningsExact identifier
application number: M017
Hempvana Maximum Strength Pain ReliefTROLAMINE SALICYLATETELEBRANDS CORPd91a0fad-a38c-1580-e053-2a95a90ad2682024-11-20WarningsExact identifier
application number: M017
Hempvana Maximum Strength Pain Relief - PlatinumTROLAMINE SALICYLATETELEBRANDS CORPd58da6c5-47a6-b8a8-e053-2995a90a7ce72024-11-20WarningsExact identifier
application number: M017
Hempvana Knee Bird Ultra Strength Pain ReliefLIDOCAINE, MENTHOLTELEBRANDS CORPdf5d3312-cbc5-5db9-e053-2995a90ab0552024-11-20WarningsExact identifier
application number: M017
Hempvana Cold as Ice GelMENTHOLTelebrands Corpa9e103f2-778f-e49b-e053-2a95a90aa8b72024-11-20WarningsExact identifier
application number: M017
Hempvana Knee Bird Ultra Strength Pain ReliefLIDOCAINE, MENTHOLTELEBRANDS CORPd58e2c47-c0f4-625e-e053-2a95a90aa4d52024-11-20WarningsExact identifier
application number: M017
Hempvana Pain ReliefTROLAMINE SALICYLATETelebrands Corp92a29553-a102-0a0e-e053-2a95a90ab24a2024-11-20WarningsExact identifier
application number: M017
Ultra Strength Pain Relief GelMENTHOLTELEBRANDS CORPd91b2e09-550e-4968-e053-2995a90ae3232024-11-20WarningsExact identifier
application number: M017
Hempvana Ultra Strength Pain Relief CreamLIDOCAINE 4%Telebrands Corpc3162ba8-ac2d-5a65-e053-2995a90af2462024-11-20WarningsExact identifier
application number: M017
Hempvana Ultra Strength Pain ReliefLIDOCAINETELEBRANDS CORPd91ba9b1-083f-32e9-e053-2a95a90a9bd12024-11-20WarningsExact identifier
application number: M017
DynaRubPAIN RELIEVING CREAMDynarex Corporation7f853941-a2d7-ed26-e053-2991aa0aa9ee2024-11-20WarningsExact identifier
application number: M017
MYCO Clinic Pain ReliefCAMPHOR, MENTHOLAidance Scientific, Inc., DBA Aidance Skincare & Topical Solutionsbcdc0322-bc75-4662-9c5a-d1be1d0552522024-11-20WarningsExact identifier
application number: M017
MYCO Clinic Pain ReliefMENTHOLAidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions604a30c9-2306-47a1-bd31-94b63639dd902024-11-20WarningsExact identifier
application number: M017
MYCO Clinic Pain ReliefCAMPHOR, MENTHOLAidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions0b489420-3b5c-43c5-aab4-0e3720acf9ce2024-11-20WarningsExact identifier
application number: M017
MYCO Clinic Pain ReliefCAMPHOR, MENTHOLAidance Scientific, Inc., DBA Aidance Skincare & Topical Solutionsdd906129-a787-4352-856d-d7a915031a6e2024-11-20WarningsExact identifier
application number: M017
Walgreens Arthritis Pain Relief CreamHISTAMINE DIHYDROCHLORIDEWalgreens Company80d3031a-7fa9-4f5b-b85e-c7c6ef3148012024-11-20WarningsExact identifier
application number: M017
Anti-Itch Medicated Maximum StrengthBENZOCAINE AND RESORCINOLWalgreens Company7fd86dcb-edef-4d0d-b389-7ecea595fe672024-11-20WarningsExact identifier
application number: M017
Walgreens Pain ReliefBENZOCAINEWalgreens Company7cee7234-32cd-4bf3-8a6c-0882585eec7f2024-11-20WarningsExact identifier
application number: M017
Walgreens Advanced Scar GelADVANCED SCAR GELWalgreens Company2c040475-a124-485c-933e-66b452f5ab462024-11-20WarningsExact identifier
application number: M017
LidoPro Pain ReliefCAPSAICIN AND LIDOCAINEClinic Pharma274611ea-7fc2-ba3f-e063-6294a90aa50f2024-11-19WarningsExact 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