Home NDC 71262-006 Prolayed Lidocaine Male Genital Desensitizer
Product NDC 71262-006
11-digit product format 712620006
Labeler code 71262
Product ID 71262-006_0b81a020-0873-e454-e063-6294a90a2e03
Type HUMAN OTC DRUG
Nonproprietary name LIDOCAINE
Dosage form OINTMENT
Route TOPICAL
Labeler ViaDerma Distribution, Inc.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-06-23
Substance LIDOCAINE
Active strength 10 mg/mL
Pharmacologic classes Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
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 Prolayed Lidocaine Male Genital Desensitizer
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE 10 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 98PI200987 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71262-006-15 Prolayed Lidocaine Male Genital Desensitizer 15 mL in 1 BOTTLE OINTMENT 15 3 71262-006-15 Prolayed Lidocaine Male Genital Desensitizer 1 in 1 BOX OINTMENT 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71262-006 PROLAYED LIDOCAINE MALE GENITAL DESENSITIZER (LIDOCAINE) OINTMENT [VIADERMA DISTRIBUTION, INC.] 3 Current NDC, Legacy NDC, 2 package rows 20231203_9c5ad0d0-ca7a-4321-9334-f06f3f6be18f.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 18 of 153 · 3,057 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 71262-006-15 71262000615 1 BOTTLE in 1 BOX (71262-006-15) / 15 mL in 1 BOTTLE 1 bottle 2017-06-23 0000-00-00 No No Current