HerX NDC 43742-1297

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1297Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1297Add 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
43742-1297-1	43742129701	30 mL in 1 BOTTLE, DROPPER (43742-1297-1)Marketed from Jul 16, 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): HerX
Generic name (nonproprietary): echinacea (angustifolia), arnica montana, hydrastis canadensis, ledum palustre, magnesia sulphurica, kalmia latifolia, arsenicum album, cocculus indicus, phosphorus
Active ingredients: Echinacea angustifolia whole — 3 [hp_X]/mLArnica montana whole — 6 [hp_X]/mLGoldenseal — 6 [hp_X]/mLRhododendron tomentosum leafy twig — 6 [hp_X]/mLMagnesium sulfate heptahydrate — 6 [hp_X]/mLKalmia latifolia leaf — 8 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLAnamirta cocculus seed — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 16, 2018
Listing expires: Dec 31, 2026
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 43742-1297_24881435-bd37-4a29-9530-f1138e91c458SPL ID 24881435-bd37-4a29-9530-f1138e91c458SPL set ID ae270bbf-40c8-44e9-91ea-ee5ddbdd9f54UNII VB06AV5US8, O80TY208ZW, ZW3Z11D0JV, 877L01IZ0P, SK47B8698T, 79N6542N18, S7V92P67HO, 810258W28U, 27YLU75U4WUPC 0810151882253
Pharmacologic class: Calculi Dissolution Agent; Osmotic Laxative

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

N443742129701 followed by a unit qualifier and the quantity

Package 43742-1297-01. 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 11, 2024.

Indications (excerpt from the label)

USES: For the temporary relief of symptoms including: • brain fog • fatigue • chills • muscle discomfort • nausea • 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)