Home NDC 80770-002 MENTHOL
Product NDC 80770-002
11-digit product format 807700002
Labeler code 80770
Product ID 80770-002_e2220f8a-ca6b-a0c8-e053-2995a90a7b80
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL
Dosage form SPRAY
Route TOPICAL
Labeler NATURAL 17
Application part341
Marketing category OTC MONOGRAPH FINAL
Marketing start 2020-10-19
Marketing end 0000-00-00
Substance MENTHOL
Active strength 2 g/100g
NDC exclude flag No
Listing certified through 2023-12-31
Current FDA listing Historical FDA.report record 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 · 4 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 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 80770-002-04 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 80770-002-04 f5e01cc5f278…a2eaf40c39c3…
FDA-Initiated Inactive NDC Indexing# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 80770-002-04 80770000204 113 g in 1 BOTTLE, SPRAY (80770-002-04) 113 g 2020-10-19 0000-00-00 No No Current