Home NDC 43742-1089 Pertussis
Product NDC 43742-1089
11-digit product format 437421089
Labeler code 43742
Product ID 43742-1089_a1ee91c3-0ca9-4129-9e5d-aa26669f24bf
Type HUMAN OTC DRUG
Nonproprietary name Aconitum Napellus, Bryonia (Alba), Hyoscyamus Niger, Ipecacuanha, Sticta Pulmonaria, Tabacum, Phosphorus, Antimonium Tartaricum, Kreosotum, Silicea, Pertussinum, Tetanus Toxin
Dosage form LIQUID
Route ORAL
Labeler Deseret Biologicals, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2017-10-31
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 4; 6; 4; 30; 30; 4; 4; 4; 5; 8; 4; 6 [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 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Pertussis
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACONITUM NAPELLUS 4 [hp_X]/mL BRYONIA ALBA ROOT 6 [hp_X]/mL HYOSCYAMUS NIGER 4 [hp_X]/mL IPECAC 30 [hp_X]/mL LOBARIA PULMONARIA 30 [hp_X]/mL TOBACCO LEAF 4 [hp_X]/mL PHOSPHORUS 4 [hp_X]/mL ANTIMONY POTASSIUM TARTRATE 4 [hp_X]/mL WOOD CREOSOTE 5 [hp_X]/mL SILICON DIOXIDE 8 [hp_X]/mL HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED 4 [hp_X]/mL CLOSTRIDIUM TETANI 6 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 12 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 43742-1089-1 Pertussis 30 mL in 1 BOTTLE, DROPPER LIQUID 30 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43742-1089 PERTUSSIS (ACONITUM NAPELLUS, BRYONIA (ALBA), HYOSCYAMUS NIGER, IPECACUANHA, STICTA PULMONARIA, TABACUM, PHOSPHORUS, ANTIMONIUM TARTARICUM, KREOSOTUM, SILICEA, PERTUSSINUM, TETANUS TOXIN) LIQUID [DESERET BIOLOGICALS, INC.] 1 Current NDC, Legacy NDC, 1 package rows 20171101_b50b5a93-dbb5-4be9-91ac-7513f0ee3410.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Pertussis ACONITUM NAPELLUS, BRYONIA (ALBA), HYOSCYAMUS NIGER, IPECACUANHA, STICTA PULMONARIA, TABACUM, PHOSPHORUS, ANTIMONIUM TARTARICUM, KREOSOTUM, SILICEA, PERTUSSINUM, TETANUS TOXIN Deseret Biologicals, Inc. b50b5a93-dbb5-4be9-91ac-7513f0ee3410 2017-10-31 Warnings Exact identifier ndc (product): 43742-1089
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 43742-1089-1 43742108901 30 mL in 1 BOTTLE, DROPPER (43742-1089-1) 30 ml 2017-10-31 0000-00-00 No No Current