Home NDC 69747-040 Greencaine Blast
Product NDC 69747-040
11-digit product format 697470040
Labeler code 69747
Product ID 69747-040_0c5b770a-fe14-17be-e063-6294a90a40a0
Type HUMAN OTC DRUG
Nonproprietary name Lidocaine
Dosage form GEL
Route TOPICAL
Labeler ALMA Laboratories, Inc.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-01-18
Substance LIDOCAINE
Active strength 40 mg/g
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 Greencaine Blast
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE 40 mg/g
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 RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1291672 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69747-040-01 Greencaine Blast 113 g in 1 TUBE GEL 113 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69747-040 GREENCAINE BLAST (LIDOCAINE) GEL [ALMA LABORATORIES, INC.] 4 Current NDC, Legacy NDC, 1 package rows 20231213_031e0065-4c8a-43d8-bc69-3efa3c6c0ae3.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 8 of 156 · 3,115 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 69747-040-01 69747004001 113 g in 1 TUBE (69747-040-01) 113 g 2018-01-18 0000-00-00 No No Current