What is NDC 43742-0949?

43742-0949 is the product NDC for Lymphoplus, Trifolium pratense flower 3 [hp_X]/mL + 9 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?

Lymphoplus (Trifolium Pratense, Lymph Node (Suis), Spleen (Suis), Conium Maculatum, Echinacea (Angustifolia), Lycopodium Clavatum, Myrrha, Phytolacca Decandra, Selenium Metallicum, Silicea).

What is the active ingredient?

Trifolium pratense flower, Sus scrofa lymph, Sus scrofa spleen, Conium maculatum flowering top, Echinacea angustifolia whole, Lycopodium clavatum spore, Myrrh, Phytolacca americana root, Selenium, Silicon dioxide.

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 Lymphoplus?

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.

Lymphoplus NDC 43742-0949 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-0949Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-0949Add 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
43742-0949-1	4374209490143742094901	30 mL in 1 BOTTLE, DROPPER (43742-0949-1)Marketed from Dec 29, 2016

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): Lymphoplus
Generic name (nonproprietary): trifolium pratense, lymph node (suis), spleen (suis), conium maculatum, echinacea (angustifolia), lycopodium clavatum, myrrha, phytolacca decandra, selenium metallicum, silicea
Active ingredients: Trifolium pratense flower — 3 [hp_X]/mLSus scrofa lymph — 8 [hp_X]/mLSus scrofa spleen — 8 [hp_X]/mLConium maculatum flowering top — 12 [hp_X]/mLEchinacea angustifolia whole — 12 [hp_X]/mLLycopodium clavatum spore — 12 [hp_X]/mLMyrrh — 12 [hp_X]/mLPhytolacca americana root — 12 [hp_X]/mLSelenium — 12 [hp_X]/mLSilicon dioxide — 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: Dec 29, 2016
Listing expires: Dec 31, 2026
Identifiers: Product ID 43742-0949_6ade7cfe-e331-4bcd-8661-11cd8b9a59c0SPL ID 6ade7cfe-e331-4bcd-8661-11cd8b9a59c0SPL set ID 92f6fc6b-58c0-4137-88b3-bee2118aeb29UNII 4JS0838828, 33A7VYU29L, 92AMN5J79Y, Q28R5GF371, VB06AV5US8, C88X29Y479, JC71GJ1F3L, 11E6VI8VEG, H6241UJ22B, ETJ7Z6XBU4UPC 0810151881102

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

N443742094901 followed by a unit qualifier and the quantity

Package 43742-0949-01. 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 May 8, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • lymph support • fever • earache • cough 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 43742-0949

What is NDC 43742-0949?: 43742-0949 is the product NDC for Lymphoplus, Trifolium pratense flower 3 [hp_X]/mL + 9 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?: Lymphoplus (Trifolium Pratense, Lymph Node (Suis), Spleen (Suis), Conium Maculatum, Echinacea (Angustifolia), Lycopodium Clavatum, Myrrha, Phytolacca Decandra, Selenium Metallicum, Silicea).
What is the active ingredient?: Trifolium pratense flower, Sus scrofa lymph, Sus scrofa spleen, Conium maculatum flowering top, Echinacea angustifolia whole, Lycopodium clavatum spore, Myrrh, Phytolacca americana root, Selenium, Silicon dioxide.
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 Lymphoplus?: 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.