Home NDC 72358-101-04 PR
Product NDC 72358-101
Requested package NDC 72358-101-04
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 · 3 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 2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 72358-101 72358-101-04 U Excluded because listing certification expired excluded / ndc_excluded.zip 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 72358-101 72358-101-04 U Excluded because listing certification expired excluded / ndc_excluded.zip ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 72358-101 72358-101-04 U Excluded because listing certification expired excluded / ndc_excluded.zip 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 53 of 151 · 3,010 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Frankincense and Myrrh Arthritis Pain Therapy MENTHOL Wise Consumer Products 2410a199-f4a3-da6c-e063-6394a90aaace 2025-12-17 Warnings Exact identifier application number: M017 Lidocaine LIDOCAINE, MENTHOL Vive Health LLC 462d3b24-643e-91da-e063-6394a90a0e1d 2025-12-17 Warnings Exact identifier application number: M017 Teevodar Pain Relieving MENTHOL Sod-e Biotech Ltd 205b0fef-4f00-db2e-e063-6294a90a93b8 2025-12-17 Warnings Exact identifier application number: M017 Frankincense and Myrrh Arthritis Pain Relief MENTHOL WISE CONSUMER PRODUCTS CO. 116045df-891b-f370-e063-6294a90abe42 2025-12-17 Warnings Exact identifier application number: M017 Frankincense and Myrrh Intensive Foot Therapy MENTHOL Wise Consumer Products 23e56c6b-0f2b-721f-e063-6394a90a1ed0 2025-12-17 Warnings Exact identifier application number: M017 Tiger Balm Ultra Strength CAMPHOR (SYNTHETIC) AND MENTHOL Haw Par Healthcare Ltd. f0561804-e0f7-495d-9768-9b86a208c51e 2025-12-17 Warnings Exact identifier application number: M017 Kwan Loong METHYL SALICYLATE AND MENTHOL Haw Par Healthcare Ltd. 54bcb26e-786a-403e-9330-11ae9e3c013a 2025-12-17 Warnings Exact identifier application number: M017 Magsoothium Body Cooling Formula MENTHOL Ubu/Elements, Inc. f7fb6ac9-a920-a440-e053-6394a90aaa35 2025-12-16 Warnings Exact identifier application number: M017 Magsoothium CBD Body Lavender MENTHOL Ubu/Elements, Inc. f9b87fbe-b889-67a1-e053-6394a90acbcd 2025-12-16 Warnings Exact identifier application number: M017 Aquaphor Itch Relief HYDROCORTISONE Beiersdorf Inc b1d0333f-ba60-35d8-e053-2995a90af932 2025-12-16 Warnings Exact identifier application number: M017 Magsoothium CBD Body MENTHOL Ubu/Elements, Inc. 00b2ef34-42d7-523c-e063-6294a90a753d 2025-12-16 Warnings Exact identifier application number: M017 GENTLECARE HAND AND SKIN SANITIZER BENZALKONIUM CHLORIDE PARAGON SOLUTIONS US, INC. 16650277-fa62-485e-9a82-7763d2b50168 2025-12-16 Warnings Exact identifier application number: M017 Welly First Aid Kit Refill HYDROCORTISONE, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, LIDOCAINE Dongguan Shenglian Tins Products Co., Ltd. 4bc93855-4009-4b49-9fb4-e5864054153d 2025-12-16 Warnings Exact identifier application number: M017 LidocainePain pain reliving gel-patch PAIN RELIVING GEL-PATCH Shenzhen Yuetai Electronic Commerce Co., Ltd 461ebbdd-0f26-a333-e063-6394a90a7a3e 2025-12-16 Warnings Exact identifier application number: M017 Zestama CAPSAICIN V2 Pharma LLC c9b46759-b8df-4ff4-815e-8e032c2635c0 2025-12-15 Warnings Exact identifier application number: M017 equate hydrocortisone HYDROCORTISONE Wal-Mart Stores Inc 70f4636d-4137-498b-ab81-0330de883e53 2025-12-15 Warnings Exact identifier application number: M017 SALONPAS-HOT CAPSICUM CAPSAICIN Hisamitsu Pharmaceutical Co., Inc. ef5373aa-9857-4d01-95af-2d7716e54ae4 2025-12-15 Warnings Exact identifier application number: M017 First Aid Burn Cream FIRST AID BURN CREAM ProStat First Aid LLC f70a442e-7ba7-4860-e053-6394a90ac2bd 2025-12-15 Warnings Exact identifier application number: M017 Burn Ease, 3.5g BURN EASE, 3.5G ProStat First Aid LLC 004aa18f-3a97-f454-e063-6394a90afcff 2025-12-15 Warnings Exact identifier application number: M017 PS-3866 Burn Ease, 0.9g PS-3866 BURN EASE, 0.9G ProStat First Aid LLC 004d00a5-9cff-29ff-e063-6294a90aeb8c 2025-12-15 Warnings Exact identifier application number: M017
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 72358-101-04 72358010104 300 g in 1 BOTTLE, PLASTIC (72358-101-04) 300 g 2018-11-01 0000-00-00 No No Current