Chestal Adult Pellets NDC 0220-9065

NDC codes

FDA NDC Directory

Product NDC (as listed)0220-9065Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00220-9065Add 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
0220-9065-41	00220906541	80 PELLET in 1 TUBE (0220-9065-41)Marketed from Jun 19, 2020
0220-9065-42	00220906542	2 TUBE in 1 BOX (0220-9065-42) / 80 PELLET in 1 TUBEMarketed from Sep 14, 2020

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): Chestal Adult Pellets
Generic name (nonproprietary): antimony potassium tartrate,bryonia alba root, protortonia cacti, drosera rotundifolia whole, ipecac, rumex crispus root, spongia officinalis skeleton, roasted, pulsatilla vulgaris whole, lobaria pulmonaria
Active ingredients: Lobaria pulmonaria — 3 [hp_C]/1Spongia officinalis skeleton, Roasted — 3 [hp_C]/1Antimony potassium tartrate — 6 [hp_C]/1Protortonia cacti — 3 [hp_C]/1Bryonia alba root — 3 [hp_C]/1Drosera rotundifolia — 3 [hp_C]/1Ipecac — 3 [hp_C]/1Pulsatilla vulgaris — 6 [hp_C]/1Rumex crispus root — 6 [hp_C]/1
Dosage form: Pellet
Route: Oral
Labeler: Boiron
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 19, 2020
Listing expires: Dec 31, 2026
Identifiers: Product ID 0220-9065_1136761e-f7a8-a719-e063-6294a90aebc3SPL ID 1136761e-f7a8-a719-e063-6294a90aebc3SPL set ID a84e27cd-8e21-0fce-e053-2a95a90af2cfUNII D1YM0P5Z2T, 1PIP394IID, DL6OZ476V3, LZB7TFX1LT, T7J046YI2B, QR44N9XPJQ, 62I3C8233L, I76KB35JEV, 9N1RM2S62C

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

N400220906541 followed by a unit qualifier and the quantity

Package 00220-9065-41. 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 12, 2024.

Indications (excerpt from the label)

Uses* temporarily relieves dry cough due to minor throat and bronchial irritation as may occur with a cold helps relieve chest congestion due to common colds by loosening mucus and thinning bronchial secretions to make coughs more productive

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)