Pertussis NDC 43742-1089

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1089Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1089Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
43742-1089-1	43742108901	30 mL in 1 BOTTLE, DROPPER (43742-1089-1)Marketed from Oct 31, 2017

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Pertussis
Generic name (nonproprietary): aconitum napellus, bryonia (alba), hyoscyamus niger, ipecacuanha, sticta pulmonaria, tabacum, phosphorus, antimonium tartaricum, kreosotum, silicea, pertussinum, tetanus toxin
Active ingredients: Aconitum napellus — 4 [hp_X]/mLBryonia alba root — 4 [hp_X]/mLHyoscyamus niger — 4 [hp_X]/mLIpecac — 4 [hp_X]/mLLobaria pulmonaria — 4 [hp_X]/mLTobacco leaf — 4 [hp_X]/mLPhosphorus — 5 [hp_X]/mLAntimony potassium tartrate — 6 [hp_X]/mLWood creosote — 6 [hp_X]/mLSilicon dioxide — 8 [hp_X]/mLHuman sputum, Bordetella pertussis infected — 30 [hp_X]/mLClostridium tetani — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 31, 2017
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)
Identifiers: Product ID 43742-1089_a1ee91c3-0ca9-4129-9e5d-aa26669f24bfSPL ID a1ee91c3-0ca9-4129-9e5d-aa26669f24bfSPL set ID b50b5a93-dbb5-4be9-91ac-7513f0ee3410UNII U0NQ8555JD, T7J046YI2B, 4WRK2153H3, 62I3C8233L, D1YM0P5Z2T, 6YR2608RSU, 27YLU75U4W, DL6OZ476V3, 3JYG22FD73, ETJ7Z6XBU4, U364V64HUN, 751E8J54VM
Pharmacologic class: Non-Standardized Plant Allergenic Extract

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N443742108901 followed by a unit qualifier and the quantity

Package 43742-1089-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Oct 31, 2017.

Indications (excerpt from the label)

HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to Pertussis infection including cough, bronchial congestion, fever, and vaccination reactions.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)