Hemcalm NDC 0220-9181

NDC codes

FDA NDC Directory

Product NDC (as listed)0220-9181Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00220-9181Add 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
0220-9181-42	00220918142	2 TUBE in 1 BOX (0220-9181-42) / 80 PELLET in 1 TUBE (0220-9181-41)Marketed from May 10, 2022

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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): Hemcalm
Generic name (nonproprietary): horse chestnut, hamamelis virginiana root bark/stem bark, strychnos nux-vomica seed
Active ingredients: Strychnos nux-vomica seed — 12 [hp_X]/1Horse chestnut — 6 [hp_X]/1Hamamelis virginiana root bark/stem bark — 6 [hp_X]/1
Dosage form: Pellet
Route: Oral
Labeler: Boiron
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 10, 2022
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 0220-9181_f495f64b-c0e2-6363-e053-2a95a90a78e0SPL ID f495f64b-c0e2-6363-e053-2a95a90a78e0SPL set ID dea9bd55-8e08-2165-e053-2995a90a8e81UNII 269XH13919, 3C18L6RJAZ, T7S323PKJS
Pharmacologic class: 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

N400220918142 followed by a unit qualifier and the quantity

Package 00220-9181-42. 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 Feb 13, 2023.

Indications (excerpt from the label)

Uses* temporarily relieves symptoms of internal and external hemorrhoids such as: burning itching swelling pain discomfort helps shrink swollen hemorrhoids relieves hemorrhoid symptoms following childbirth

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)