43742-1089 : Pertussis Oral Liquid
| NDC: | 43742-1089 |
| Labeler: | Deseret Biologicals, Inc. |
| Product Type: | Human OTC Drug |
| Drug Name: | Pertussis |
| Dosage Form: | Oral Liquid |
| Rev. Date: |
NDC Package Codes:
- 43742-1089-1: 30 ML IN 1 BOTTLE, DROPPER (43742‑1089‑1)
Active Ingredients:
- Aconitum Napellus
- Bryonia Alba Root
- Hyoscyamus Niger
- Ipecac
- Lobaria Pulmonaria
- Tobacco Leaf
- Phosphorus
- Antimony Potassium Tartrate
- Wood Creosote
- Silicon Dioxide
- Human Sputum
- Bordetella Pertussis Infected
- Clostridium Tetani
Dosage Strength:
- 4 [hp_X]/mL
- 4 [hp_X]/mL
- 4 [hp_X]/mL
- 4 [hp_X]/mL
- 4 [hp_X]/mL
- 4 [hp_X]/mL
- 5 [hp_X]/mL
- 6 [hp_X]/mL
- 6 [hp_X]/mL
- 8 [hp_X]/mL
- 30 [hp_X]/mL
- 30 [hp_X]/mL
Related Products:
Based on records with the same trade name.- 43742-0400 Pertussis Oral Liquid by Deseret Biologicals, Inc.
- 43742-0723 Pertussis Oral Liquid by Deseret Biologicals, Inc.
- 43742-0916 Pertussis Oral Liquid by Deseret Biologicals, Inc.
- 43742-0989 Pertussis Oral Liquid by Deseret Biologicals, Inc.
- 43742-1320 Pertussis Oral Liquid by Deseret Biologicals, Inc.
- 43742-0203 Pertussis Oral Liquid by Deseret Biologicals, Inc
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.
