FDA.reportPublic FDA data

BODY ACTION PRODUCTS Climax Control Gel

Product NDC
70742-282
11-digit product format
707420282
Labeler code
70742
Product ID
70742-282_09d7805e-6565-5fa8-e063-6294a90ac4bb
Type
HUMAN OTC DRUG
Nonproprietary name
BENZOCAINE
Dosage form
GEL
Route
TOPICAL
Labeler
PRODUCT MAX GROUP INC
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-04-29
Substance
BENZOCAINE
Active strength
50 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
BODY ACTION PRODUCTS Climax Control Gel
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZOCAINE50 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
53e746cc-0078-4381-bf0b-9c8f98d66904Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70742-282-00BODY ACTION PRODUCTS Climax Control Gel60 mL in 1 BOTTLEGEL602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70742-282BODY ACTION PRODUCTS CLIMAX CONTROL GEL (BENZOCAINE) GEL [PRODUCT MAX GROUP INC]2Current NDC, Legacy NDC, 1 package rows20231111_53e746cc-0078-4381-bf0b-9c8f98d66904.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 125 of 151 · 3,010 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Herb Street Arthritis ReliefMENTHOL/CAMPHORBalassa Laboratories Inc.a9d8ceb7-def0-415f-8fc1-ff8dd3e418552024-10-01WarningsExact identifier
application number: M017
Lido King Lidocaine 4% Pain Relieving Gel-PatchLIDOCAINEGalaxy Bio, Inc.2243734a-4ea2-a5e5-e063-6294a90aba152024-10-01WarningsExact identifier
application number: M017
Medicated Herbal Lip BalmMENTHOLEarth Mama Angel Baby LLC1cc2391e-6a7a-609c-e063-6394a90a63052024-10-01WarningsExact identifier
application number: M017
CVS Health Lidocaine Plus Pain RelievingLIDOCAINE HYDROCHLORIDE, BENZYL ALCOHOLNATURAL ESSENTIALS, INC.1adb9b74-4a01-4461-b845-f3aedcb3f8102024-10-01WarningsExact identifier
application number: M017
CircataCAPSAICINPureTek Corporationb67161d7-cc5c-e971-e053-2995a90acbe72024-10-01WarningsExact identifier
application number: M017
MenticamCAMPHOR,MENTHOL, METHYL SALICYLATEPureTek Corporationffea2e97-777f-434b-e053-6394a90a3a632024-10-01WarningsExact identifier
application number: M017
Herb Street Sore Muscle ReliefMETHYL SALICYLATEBalassa Laboratories Inc.e43943c2-d4cd-44c5-a0ff-403a8d42860f2024-10-01WarningsExact identifier
application number: M017
hydrocortisoneHYDROCORTISONEKroger Company68dab606-0385-48b7-9a7b-a2cf83d203932024-09-29WarningsExact identifier
application number: M017
kirkland signature hydrocortisone plus maximum strengthHYDROCORTISONECostco Wholesale Company481341c5-db1f-43fb-aed7-f40495a4eab82024-09-29WarningsExact identifier
application number: M017
Care One hydrocortisone maximum strengthHYDROCORTISONEAmerican Sales Company32593229-d0ac-4d6c-831a-089fc6e761522024-09-29WarningsExact identifier
application number: M017
good sense anti itchHYDROCORTISONEL. Perrigo Companyb7a896cc-1d78-45c0-a73e-aa1e117f7d3b2024-09-29WarningsExact identifier
application number: M017
Topcare HydrocortisoneHYDROCORTISONETopco Associates LLCb7362f21-f1a3-4edc-b5b6-a16680e05df32024-09-29WarningsExact identifier
application number: M017
hydrocortisoneHYDROCORTISONEH E B412ca2d1-064b-4438-aee1-fcb5cf27c7db2024-09-29WarningsExact identifier
application number: M017
Topcare AntibioticNEOMYCIN, POLYMYXIN B, PRAMOXINE HYDROCHLORIDETopco Associates LLC8c349cac-20e1-4600-9b0a-fcfe929551c52024-09-26WarningsExact identifier
application number: M017
good sense anti itchHYDROCORTISONEA-S Medication Solutions072dd455-24a5-4a44-aaef-d3e137d005a62024-09-26WarningsExact identifier
application number: M017
SYREN Intimate ReliefLIDOCAINE HYDROCHLORIDEIcon Health Science57d5a080-3583-4510-e053-2a91aa0ad5892024-09-25WarningsExact identifier
application number: M017
AOSI HEALTHCAREHYDROCORTISONENantong Health & Beyond Hygienic Products Inc.f4db90ad-dd62-44f1-9655-2614ed36581e2024-09-25WarningsExact identifier
application number: M017
AOSI HEALTHCARE BURNLIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDENantong Health & Beyond Hygienic Products Inc.a28b920c-0bb8-4b5a-addd-26ea164e036e2024-09-25WarningsExact identifier
application number: M017
anti itchDIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATEKroger Company067e718a-ec0b-4895-8f9f-82d64ab4c7b42024-09-24WarningsExact identifier
application number: M017
topcare anti itchDIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATETopco Associates LLCe0fb332a-2903-41ef-b35b-7cd3a74cff992024-09-24WarningsExact identifier
application number: M017

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70742-282-007074202820060 mL in 1 BOTTLE (70742-282-00) 60 ml2022-04-290000-00-00NoNoCurrent