Home NDC 81555-202-01 CELLANDIR SCALP AMPOULE
Product NDC 81555-202
Requested package NDC 81555-202-01
11-digit product format 815550202
Labeler code 81555
Product ID 81555-202_c1a17b48-9e07-ea0a-e053-2a95a90a997f
Type HUMAN OTC DRUG
Nonproprietary name Menthol, Salicylic Acid, Allantoin
Dosage form LIQUID
Route TOPICAL
Labeler H.L.C GROUP Co., ltd
Application part348
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2021-05-06
Marketing end 0000-00-00
Substance MENTHOL, UNSPECIFIED FORM; SALICYLIC ACID; ALLANTOIN
Active strength 0 mg/100mL; mg/100mL; mg/100mL
NDC exclude flag No
Listing certified through 2022-12-31
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 · 9 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
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 81555-202-01 CELLANDIR SCALP AMPOULE 50 mL in 1 AMPULE LIQUID 50 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81555-202 CELLANDIR SCALP AMPOULE (MENTHOL, SALICYLIC ACID, ALLANTOIN) LIQUID [H.L.C GROUP CO., LTD] 2 Legacy NDC, 1 package rows 20231125_c1a17b48-9e06-ea0a-e053-2a95a90a997f.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 81555-202-01 81555020201 50 mL in 1 AMPULE (81555-202-01) 50 ml 2021-05-06 0000-00-00 No No Current