What is NDC 43742-1019?

43742-1019 is the product NDC for Upper Respiratory Support, Onion 3 [hp_X]/mL + 20 more ingredients liquid, listed with the FDA by Deseret Biologicals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Upper Respiratory Support (Allium Cepa, Echinacea (Angustifolia), Eucalyptus Globulus, Salvia Officinalis, Dulcamara, Euphrasia Officinalis, Hydrastis Canadensis, Natrum Muriaticum, Sabadilla, Viscum Album, Mucosa Nasalis Suis, Aconitum Napellus, Ammonium Carbonicum, Arsenicum Iodatum, Bryonia (Alba), Gelsemium Sempervirens, Kali Bichromicum, Mercurius Vivus, Nux Vomica, Pulsatilla (Pratensis), Rhus Tox).

What is the active ingredient?

Onion, Echinacea angustifolia whole, Eucalyptus globulus leaf, Sage, Solanum dulcamara top, Euphrasia stricta, Goldenseal, Sodium chloride, Schoenocaulon officinale seed, Viscum album fruiting top, Sus scrofa nasal mucosa, Aconitum napellus whole, Ammonium carbonate, Arsenic trioxide, Bryonia alba root, Gelsemium sempervirens root, Potassium dichromate, Mercury, Strychnos nux-vomica seed, Pulsatilla pratensis whole, Toxicodendron pubescens leaf.

Deseret Biologicals, Inc., NDC labeler code 43742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Upper Respiratory Support?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Upper Respiratory Support NDC 43742-1019

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1019Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1019Add 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
43742-1019-1	4374210190143742101901	30 mL in 1 BOTTLE, DROPPER (43742-1019-1)Marketed from Jun 6, 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): Upper Respiratory Support
Generic name (nonproprietary): allium cepa, echinacea (angustifolia), eucalyptus globulus, salvia officinalis, dulcamara, euphrasia officinalis, hydrastis canadensis, natrum muriaticum, sabadilla, viscum album, mucosa nasalis suis, aconitum napellus, ammonium carbonicum, arsenicum iodatum, bryonia (alba), gelsemium sempervirens, kali bichromicum, mercurius vivus, nux vomica, pulsatilla (pratensis), rhus tox
Active ingredients: Onion — 3 [hp_X]/mLEchinacea angustifolia whole — 3 [hp_X]/mLEucalyptus globulus leaf — 3 [hp_X]/mLSage — 3 [hp_X]/mLSolanum dulcamara top — 6 [hp_X]/mLEuphrasia stricta — 6 [hp_X]/mLGoldenseal — 6 [hp_X]/mLSodium chloride — 6 [hp_X]/mLSchoenocaulon officinale seed — 6 [hp_X]/mLViscum album fruiting top — 6 [hp_X]/mLSus scrofa nasal mucosa — 6 [hp_X]/mLAconitum napellus whole — 12 [hp_X]/mLAmmonium carbonate — 12 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLBryonia alba root — 12 [hp_X]/mLGelsemium sempervirens root — 12 [hp_X]/mLPotassium dichromate — 12 [hp_X]/mLMercury — 12 [hp_X]/mLStrychnos nux-vomica seed — 12 [hp_X]/mLPulsatilla pratensis whole — 12 [hp_X]/mLToxicodendron pubescens leaf — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.NDC labeler code 43742
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 6, 2017
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 43742-1019_ae7969d2-5d4c-4cc3-b227-e6baf9d98025SPL ID ae7969d2-5d4c-4cc3-b227-e6baf9d98025SPL set ID 882a284f-aa25-40cf-8aff-fe4c38ff3f0aUNII 492225Q21H, VB06AV5US8, S546YLW6E6, 065C5D077J, KPS1B1162N, C9642I91WL, ZW3Z11D0JV, 451W47IQ8X, 6NAF1689IO, BK9092J5MP, ID3Z1X61WY, U0NQ8555JD, NJ5VT0FKLJ, S7V92P67HO, T7J046YI2B, 639KR60Q1Q, T4423S18FM, FXS1BY2PGL, 269XH13919, 8E272251DI, 6IO182RP7AUPC 0810151882123
Pharmacologic class: Non-Standardized Food Allergenic Extract; 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

N443742101901 followed by a unit qualifier and the quantity

Package 43742-1019-01. 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 Aug 23, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • upper respiratory support • cough • sneezing • runny nose • fatigue • body aches • brain fog • sinus congestion • malaise 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)

About NDC 43742-1019

What is NDC 43742-1019?: 43742-1019 is the product NDC for Upper Respiratory Support, Onion 3 [hp_X]/mL + 20 more ingredients liquid, listed with the FDA by Deseret Biologicals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Upper Respiratory Support (Allium Cepa, Echinacea (Angustifolia), Eucalyptus Globulus, Salvia Officinalis, Dulcamara, Euphrasia Officinalis, Hydrastis Canadensis, Natrum Muriaticum, Sabadilla, Viscum Album, Mucosa Nasalis Suis, Aconitum Napellus, Ammonium Carbonicum, Arsenicum Iodatum, Bryonia (Alba), Gelsemium Sempervirens, Kali Bichromicum, Mercurius Vivus, Nux Vomica, Pulsatilla (Pratensis), Rhus Tox).
What is the active ingredient?: Onion, Echinacea angustifolia whole, Eucalyptus globulus leaf, Sage, Solanum dulcamara top, Euphrasia stricta, Goldenseal, Sodium chloride, Schoenocaulon officinale seed, Viscum album fruiting top, Sus scrofa nasal mucosa, Aconitum napellus whole, Ammonium carbonate, Arsenic trioxide, Bryonia alba root, Gelsemium sempervirens root, Potassium dichromate, Mercury, Strychnos nux-vomica seed, Pulsatilla pratensis whole, Toxicodendron pubescens leaf.
Who is the labeler?: Deseret Biologicals, Inc., NDC labeler code 43742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Upper Respiratory Support?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.