Home NDC 65923-104 Family Care Maximum Strength Medicated Anti Itch
Product NDC 65923-104
11-digit product format 659230104
Labeler code 65923
Product ID 65923-104_41b455e2-0768-80cb-e063-6394a90a5698
Type HUMAN OTC DRUG
Nonproprietary name Menthol
Dosage form CREAM
Route TOPICAL
Labeler United Exchange Corp.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2014-11-24
Substance MENTHOL; PRAMOXINE HYDROCHLORIDE
Active strength 10; 10 mg/g; mg/g
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 Family Care Maximum Strength Medicated Anti Itch
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 10 mg/g PRAMOXINE HYDROCHLORIDE 10 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L7T10EIP3A Internal UNII lookup 88AYB867L5 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1116155 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 65923-104-14 Family Care Maximum Strength Medicated Anti Itch 1 in 1 CARTON CREAM 1 16 65923-104-14 Family Care Maximum Strength Medicated Anti Itch 14 g in 1 TUBE CREAM 14 16
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 65923-104 FAMILY CARE MAXIMUM STRENGTH MEDICATED ANTI ITCH (MENTHOL) CREAM [UNITED EXCHANGE CORP.] 14 Current NDC, Legacy NDC, 2 package rows 20250305_430b5753-3087-4cb1-bf54-0eedc3f4b1d5.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.
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 65923-104-14 65923010414 1 TUBE in 1 CARTON (65923-104-14) / 14 g in 1 TUBE 1 tube 2018-10-30 0000-00-00 No No Current