Home NDC 72184-001-01 Theresienol MD Skin Protectant
Product NDC 72184-001
Requested package NDC 72184-001-01
11-digit product format 721840001
Labeler code 72184
Product ID 72184-001_c88df38f-6f33-3e76-e053-2995a90a468f
Type HUMAN OTC DRUG
Nonproprietary name Lanolin
Dosage form LIQUID
Route TOPICAL
Labeler Fordee Group, LLC
Application part347
Marketing category OTC MONOGRAPH FINAL
Marketing start 2018-03-26
Marketing end 2025-07-31
Substance LANOLIN
Active strength 13 g/100mL
NDC exclude flag No
Listing certified through 0000-00-00
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 · 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 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 72184-001 72184-001-01 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 72184-001 72184-001-01 D Discontinued by firm excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72184-001 THERESIENOL MD SKIN PROTECTANT (LANOLIN) LIQUID [FORDEE GROUP, LLC] 3 Legacy NDC 20210802_6855c562-ecdb-5e82-e053-2a91aa0a2d40.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 72184-001-01 72184000101 10 PACKET in 1 CARTON (72184-001-01) > 1 mL in 1 PACKET 10 packet 2018-03-26 2025-07-31 No No Current