Home NDC 43742-0781-1 Apiol
Product NDC 43742-0781
Requested package NDC 43742-0781-1
11-digit product format 437420781
Labeler code 43742
Product ID 43742-0781_40dd015b-02b6-4dae-a802-6efa7a10ef0d
Type HUMAN OTC DRUG
Nonproprietary name Apiolum
Dosage form LIQUID
Route ORAL
Labeler Deseret Biologicals, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2016-06-29
Marketing end 0000-00-00
Substance APIOLE (PARSLEY)
Active strength 6 [hp_X]/mL
NDC exclude flag No
Listing certified through 2024-12-31
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 · 1 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 43742-0781 43742-0781-1 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43742-0781 APIOL (APIOLUM) LIQUID [DESERET BIOLOGICALS, INC.] 4 Legacy NDC 20250529_aea6b523-29fa-4392-ae57-d5038404fd47.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 43742-0781-1 43742078101 30 mL in 1 BOTTLE, DROPPER (43742-0781-1) 30 ml 2016-06-29 0000-00-00 No No Current