Home NDC 72358-101 PR
Product NDC 72358-101
11-digit product format 723580101
Labeler code 72358
Product ID 72358-101_4229f4ae-8934-0e10-e063-6394a90a4185
Type HUMAN OTC DRUG
Nonproprietary name Menthol
Dosage form LOTION
Route TOPICAL
Labeler Amphp, Inc
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-11-01
Substance MENTHOL
Active strength .5 g/100g
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 · 9 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-02-02 03:52 UTC · source 2025-01-31 excluded product product 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 72358-101-04 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 72358-101-03 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 72358-101-04 ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 72358-101-03 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 72358-101-04 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 72358-101-03 0efc9e666f02…f202fb6c5f17…
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 PR
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL .5 g/100g
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 1293193 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 72358-101-03 PR 20 g in 1 PACKET LOTION 20 9 72358-101-04 PR 300 g in 1 BOTTLE, PLASTIC LOTION 300 9
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72358-101 PR (MENTHOL) LOTION [AMPHP, INC] 8 Current NDC, Legacy NDC, 2 package rows 20250305_6f5b9e08-c445-4fac-e053-2a91aa0aa737.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 72358-101-01 72358010101 300 g in 1 TUBE (72358-101-01) 300 g 2018-11-01 0000-00-00 No No Current 72358-101-02 72358010102 100 g in 1 TUBE (72358-101-02) 100 g 2018-11-01 0000-00-00 No No Current 72358-101-03 72358010103 20 g in 1 PACKET (72358-101-03) 20 g 2018-11-01 0000-00-00 No No Current 72358-101-04 72358010104 300 g in 1 BOTTLE, PLASTIC (72358-101-04) 300 g 2018-11-01 0000-00-00 No No Current