What is NDC 0220-9115?

0220-9115 is the product NDC for Chestal Cough And Mucus, Spongia officinalis skeleton, Roasted 3 [hp_C]/1 + 8 more ingredients tablet, listed with the FDA by Boiron. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Chestal Cough And Mucus (Antimony potassium tartrate, Bryonia alba root, Protortonia cacti, Drosera rotundifolia, Ipecac, Pulsatilla vulgaris whole, Rumex crispus root, Spongia officinalis skeleton, Roasted, Lobaria pulmonaria).

What is the active ingredient?

Spongia officinalis skeleton, Roasted, Ipecac, Rumex crispus root, Lobaria pulmonaria, Protortonia cacti, Drosera rotundifolia, Pulsatilla vulgaris whole, Antimony potassium tartrate, Bryonia alba root.

Boiron, NDC labeler code 0220. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Chestal Cough And Mucus?

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.

Chestal Cough And Mucus NDC 0220-9115 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)0220-9115Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00220-9115Add 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
0220-9115-04	00220911504	3 BLISTER PACK in 1 CARTON (0220-9115-04) / 20 TABLET in 1 BLISTER PACKMarketed from Mar 20, 2026

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 Cough And Mucus
Generic name (nonproprietary): antimony potassium tartrate, bryonia alba root, protortonia cacti, drosera rotundifolia, ipecac, pulsatilla vulgaris whole, rumex crispus root, spongia officinalis skeleton, roasted, lobaria pulmonaria
Active ingredients: Spongia officinalis skeleton, Roasted — 3 [hp_C]/1Ipecac — 3 [hp_C]/1Rumex crispus root — 6 [hp_C]/1Lobaria pulmonaria — 3 [hp_C]/1Protortonia cacti — 3 [hp_C]/1Drosera rotundifolia — 3 [hp_C]/1Pulsatilla vulgaris whole — 6 [hp_C]/1Antimony potassium tartrate — 6 [hp_C]/1Bryonia alba root — 3 [hp_C]/1
Dosage form: Tablet
Route: Oral
Labeler: BoironNDC labeler code 0220
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 20, 2026
Listing expires: Dec 31, 2027
Identifiers: Product ID 0220-9115_4d77a058-e6c9-2af5-e063-6394a90afe1aSPL ID 4d77a058-e6c9-2af5-e063-6394a90afe1aSPL set ID 4d77a058-e6c8-2af5-e063-6394a90afe1aUNII 1PIP394IID, 62I3C8233L, 9N1RM2S62C, D1YM0P5Z2T, LZB7TFX1LT, QR44N9XPJQ, I76KB35JEV, DL6OZ476V3, T7J046YI2B

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

N400220911504 followed by a unit qualifier and the quantity

Package 00220-9115-04. 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 20, 2026.

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)

About NDC 0220-9115

What is NDC 0220-9115?: 0220-9115 is the product NDC for Chestal Cough And Mucus, Spongia officinalis skeleton, Roasted 3 [hp_C]/1 + 8 more ingredients tablet, listed with the FDA by Boiron. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Chestal Cough And Mucus (Antimony potassium tartrate, Bryonia alba root, Protortonia cacti, Drosera rotundifolia, Ipecac, Pulsatilla vulgaris whole, Rumex crispus root, Spongia officinalis skeleton, Roasted, Lobaria pulmonaria).
What is the active ingredient?: Spongia officinalis skeleton, Roasted, Ipecac, Rumex crispus root, Lobaria pulmonaria, Protortonia cacti, Drosera rotundifolia, Pulsatilla vulgaris whole, Antimony potassium tartrate, Bryonia alba root.
Who is the labeler?: Boiron, NDC labeler code 0220. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Chestal Cough And Mucus?: 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.