Home NDC 43742-1320-1 Pertussis
Product NDC 43742-1320
Requested package NDC 43742-1320-1
11-digit product format 437421320
Labeler code 43742
Product ID 43742-1320_1ab03905-9088-4cfe-bac8-b57ce2c82163
Type HUMAN OTC DRUG
Nonproprietary name Ipecacuanha, Sticta Pulmonaria, Phosphorus, Antimonium Tartaricum, Kreosotum, Aconitum Napellus, Bryonia (Alba), Hyoscyamus Niger, Silicea, Tabacum, Pertussinum, Tetanus Toxin
Dosage form LIQUID
Route ORAL
Labeler Deseret Biologicals, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2018-09-04
Marketing end 2025-05-13
Substance ACONITUM NAPELLUS; ANTIMONY POTASSIUM TARTRATE; BRYONIA ALBA ROOT; CLOSTRIDIUM TETANI; HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED; HYOSCYAMUS NIGER; IPECAC; LOBARIA PULMONARIA; PHOSPHORUS; SILICON DIOXIDE; TOBACCO LEAF; WOOD CREOSOTE
Active strength 8 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS]
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 43742-1320 43742-1320-1 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 43742-1320 43742-1320-1 D Discontinued by firm excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
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 43742-1320-1 43742132001 30 mL in 1 BOTTLE, DROPPER (43742-1320-1) 30 ml 2018-09-04 2025-05-13 No No Current