Pertussis
- Product NDC
- 43742-0400
- 11-digit product format
- 437420400
- Labeler code
- 43742
- Product ID
- 43742-0400_5a0514c1-ce83-47e5-9764-15932a20f350
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aconitum napellus, Antimonium tartaricum, Belladonna, Bryonia (Alba), Hyoscyamus niger, Ipecacuanha, Lobelia inflata, Sticta pulmonaria, Phosphorus,
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-06-12
- Marketing end
- 2020-07-28
- Substance
- ACONITUM NAPELLUS; ANTIMONY POTASSIUM TARTRATE; ATROPA BELLADONNA; BRYONIA ALBA ROOT; HYOSCYAMUS NIGER; IPECAC; LOBELIA INFLATA; LOBARIA PULMONARIA; PHOSPHORUS; WOOD CREOSOTE; SILICON DIOXIDE; HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED; CLOSTRIDIUM TETANI
- Active strength
- 4 [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; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record