Home NDC 24470-965 LIDOCAINE HYDROCHLORIDE, HYDROCORTISONE ACETATE
Product NDC 24470-965
11-digit product format 244700965
Labeler code 24470
Product ID 24470-965_2251cadf-fe7a-340c-e063-6394a90a296a
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name LIDOCAINE HYDROCHLORIDE, HYDROCORTISONE ACETATE
Dosage form CREAM
Route RECTAL
Labeler Cintex Services, LLC
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2024-09-11
Substance HYDROCORTISONE ACETATE; LIDOCAINE HYDROCHLORIDE
Active strength 5; 30 mg/g; mg/g
Pharmacologic classes Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Local Anesthesia [PE]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base LIDOCAINE HYDROCHLORIDE, HYDROCORTISONE ACETATE
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE HYDROCHLORIDE 5 mg/g HYDROCORTISONE ACETATE 30 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination V13007Z41A Internal UNII lookup 3X7931PO74 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1012235 Internal RxNorm 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 24470-965-01 LIDOCAINE HYDROCHLORIDE, HYDROCORTISONE ACETATE 7 g in 1 TUBE CREAM 7 2 24470-965-20 LIDOCAINE HYDROCHLORIDE, HYDROCORTISONE ACETATE 20 in 1 KIT CREAM 20 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 24470-965 LIDOCAINE HYDROCHLORIDE, HYDROCORTISONE ACETATE CREAM [CINTEX SERVICES, LLC] 2 Current NDC, 2 package rows 20240919_21dee088-0fb0-ecd0-e063-6294a90a0e57.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 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 24470-965-01 24470096501 7 g in 1 TUBE 7 g Historical 24470-965-20 24470096520 20 TUBE in 1 KIT (24470-965-20) / 7 g in 1 TUBE (24470-965-01) 20 tube 2024-09-11 No No Current