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 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

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