Breathe NDC 43742-1263

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1263Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1263Add 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
43742-1263-1	43742126301	30 mL in 1 BOTTLE, DROPPER (43742-1263-1)Marketed from Nov 14, 2018

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): Breathe
Generic name (nonproprietary): argentum nitricum, natrum muriaticum, sulphur, aconitum napellus, arsenicum album, rhus tox, adenosinum cyclophosphoricum, funiculus umbilicalis suis, glandula suprarenalis suis, lung (suis), mucosa nasalis suis, pantothenic acid, sarcolacticum acidum, acetylcholine chloride, coumarinum, malvin, dysentery bacillus, proteus (morgani)
Active ingredients: Silver nitrate — 6 [hp_X]/mLSodium chloride — 6 [hp_X]/mLSulfur — 6 [hp_X]/mLAconitum napellus — 8 [hp_X]/mLArsenic trioxide — 8 [hp_X]/mLToxicodendron pubescens leaf — 8 [hp_X]/mLAdenosine cyclic phosphate — 10 [hp_X]/mLSus scrofa umbilical cord — 10 [hp_X]/mLSus scrofa adrenal gland — 10 [hp_X]/mLSus scrofa lung — 10 [hp_X]/mLSus scrofa nasal mucosa — 10 [hp_X]/mLPantothenic acid — 10 [hp_X]/mLLactic acid, L- — 10 [hp_X]/mLAcetylcholine chloride — 6 [hp_C]/mLCoumarin — 6 [hp_C]/mLMalvin — 15 [hp_C]/mLShigella dysenteriae — 30 [hp_C]/mLProteus morganii — 30 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 14, 2018
Listing expires: Dec 31, 2026
Other FDA classes: Cholinergic Agonists (Mechanism)
Identifiers: Product ID 43742-1263_e847b14d-de88-4d5d-8fba-c528919bbfc8SPL ID e847b14d-de88-4d5d-8fba-c528919bbfc8SPL set ID 8dbdd623-a486-4cf8-acdb-ad051dc74348UNII 95IT3W8JZE, 451W47IQ8X, 70FD1KFU70, U0NQ8555JD, S7V92P67HO, 6IO182RP7A, E0399OZS9N, 118OYG6W3H, 398IYQ16YV, 7GL3G1COB3, ID3Z1X61WY, 19F5HK2737, F9S9FFU82N, AF73293C2R, A4VZ22K1WT, I9I120531L, 1EP6R5562J, 56X6LID5ZYUPC 0810151881478
Pharmacologic class: Cholinergic Receptor Agonist

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

N443742126301 followed by a unit qualifier and the quantity

Package 43742-1263-01. 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 Mar 15, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • minor breathing issues • lung support 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)