Home NDC 73598-1202 CHERRY COUGH DROPS 50CT
Product NDC 73598-1202
11-digit product format 735981202
Labeler code 73598
Product ID 73598-1202_3881b210-89b4-4979-a2d1-f09881a7b948
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL, UNSPECIFIED FORM
Dosage form LOZENGE
Route ORAL
Labeler JHK Inc dba American Safety & First Aid
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2000-02-02
Substance MENTHOL, UNSPECIFIED FORM
Active strength 7.6 mg/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2024-03-11 06:39 UTC · source 2024-03-08 excluded product product 73598-1202 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 73598-1202 73598-1202-1 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…
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 CHERRY COUGH DROPS 50CT
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL, UNSPECIFIED FORM 7.6 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L7T10EIP3A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 359751 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 73598-1202-1 CHERRY COUGH DROPS 50CT 50 in 1 BOX LOZENGE 50 2 73598-1202-1 CHERRY COUGH DROPS 50CT 1 in 1 PACKET LOZENGE 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73598-1202 CHERRY COUGH DROPS 50CT (MENTHOL, UNSPECIFIED FORM) LOZENGE CHERRY COUGH DROPS 100CT (MENTHOL, UNSPECIFIED FORM) LOZENGE [JHK INC DBA AMERICAN SAFETY & FIRST AID] 2 Current NDC, Legacy NDC, 2 package rows 20240426_2f54b9c1-3a37-48fd-b964-6aa2631b8e62.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 97 of 178 · 3,551 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 73598-1202-1 73598120201 50 PACKET in 1 BOX (73598-1202-1) / 1 LOZENGE in 1 PACKET 50 packet 2000-02-02 0000-00-00 No No Current