Home NDC 70742-282 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 Ingredient Strength BENZOCAINE 50 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination U3RSY48JW5 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70742-282-00 BODY ACTION PRODUCTS Climax Control Gel 60 mL in 1 BOTTLE GEL 60 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70742-282 BODY ACTION PRODUCTS CLIMAX CONTROL GEL (BENZOCAINE) GEL [PRODUCT MAX GROUP INC] 2 Current NDC, Legacy NDC, 1 package rows 20231111_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 108 of 151 · 3,020 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 70742-282-00 70742028200 60 mL in 1 BOTTLE (70742-282-00) 60 ml 2022-04-29 0000-00-00 No No Current