What is NDC 72968-0003?

72968-0003 is the product NDC for Herplex, Chrysopogon zizanioides root 12 [hp_X]/1 + 8 more ingredients tablet, listed with the FDA by Nashco Products LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Herplex (Anatherum Muricatum, Clematis Erecta, Mezereum, Phytolacca Decandra, Ranunculus Bulbosus, Rhus Tox, Thuja Occidentalis, Natrum Muriaticum, Sepia).

What is the active ingredient?

Chrysopogon zizanioides root, Clematis recta flowering top, Daphne mezereum bark, Phytolacca americana root, Ranunculus bulbosus whole, Toxicodendron pubescens leaf, Thuja occidentalis leafy twig, Sodium chloride, Sepia officinalis juice.

Nashco Products LLC, NDC labeler code 72968. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Herplex?

2 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Herplex NDC 72968-0003 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72968-0003Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72968-0003Add 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
72968-0003-1	7296800030172968000301	60 TABLET in 1 BOTTLE, PLASTIC (72968-0003-1)Marketed from Jul 11, 2022

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): Herplex
Generic name (nonproprietary): anatherum muricatum, clematis erecta, mezereum, phytolacca decandra, ranunculus bulbosus, rhus tox, thuja occidentalis, natrum muriaticum, sepia
Active ingredients: Chrysopogon zizanioides root — 12 [hp_X]/1Clematis recta flowering top — 12 [hp_X]/1Daphne mezereum bark — 12 [hp_X]/1Phytolacca americana root — 12 [hp_X]/1Ranunculus bulbosus whole — 12 [hp_X]/1Toxicodendron pubescens leaf — 12 [hp_X]/1Thuja occidentalis leafy twig — 12 [hp_X]/1Sodium chloride — 30 [hp_X]/1Sepia officinalis juice — 30 [hp_X]/1
Dosage form: Tablet
Route: Oral
Labeler: Nashco Products LLCNDC labeler code 72968
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 11, 2022
Listing expires: Dec 31, 2027
Identifiers: Product ID 72968-0003_f5ad27ec-888c-49f0-ac00-2a10cbf72cc3SPL ID f5ad27ec-888c-49f0-ac00-2a10cbf72cc3SPL set ID e5e7aa2f-3697-4747-9045-670ea2b13557UNII 37TB8LUP9Z, 396421SP9F, X2N6E405GV, 11E6VI8VEG, AEQ8NXJ0MB, 6IO182RP7A, 1NT28V9397, 451W47IQ8X, QDL83WN8C2

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

N472968000301 followed by a unit qualifier and the quantity

Package 72968-0003-01. 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 14, 2026.

Indications (excerpt from the label)

USES: **Temporarily relieve pain and itching during ■ outbreaks of cold sores and fever blisters. **CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72968-0003

What is NDC 72968-0003?: 72968-0003 is the product NDC for Herplex, Chrysopogon zizanioides root 12 [hp_X]/1 + 8 more ingredients tablet, listed with the FDA by Nashco Products LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Herplex (Anatherum Muricatum, Clematis Erecta, Mezereum, Phytolacca Decandra, Ranunculus Bulbosus, Rhus Tox, Thuja Occidentalis, Natrum Muriaticum, Sepia).
What is the active ingredient?: Chrysopogon zizanioides root, Clematis recta flowering top, Daphne mezereum bark, Phytolacca americana root, Ranunculus bulbosus whole, Toxicodendron pubescens leaf, Thuja occidentalis leafy twig, Sodium chloride, Sepia officinalis juice.
Who is the labeler?: Nashco Products LLC, NDC labeler code 72968. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Herplex?: 2 other product NDCs are listed under this name. See all Herplex NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Herplex NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Herplexanatherum muricatum, clematis erecta, mezereum, phytolacca decandra, ranunculus bulbosus, rhus tox, thuja occidentalis, natrum muriaticum, sepia	Chrysopogon zizanioides root 12 [hp_X]/1 + 8 more ingredients	TabletOral	Nashco Products LLC	72968-0004	72968-0004-01
Herplexanatherum muricatum, clematis erecta, mezereum, phytolacca decandra, ranunculus bulbosus, rhus tox, thuja occidentalis, natrum muriaticum, sepia	Chrysopogon zizanioides root 12 [hp_X]/1 + 8 more ingredients	TabletOral	Nashco Products LLC	72968-0002	72968-0002-01