Chestal NDC 0220-9032

NDC codes

FDA NDC Directory

Product NDC (as listed)0220-9032Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00220-9032Add 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
0220-9032-28	00220903228	200 mL in 1 BOTTLE (0220-9032-28)Marketed from Feb 1, 1993

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
Generic name (nonproprietary): antimony potassium tartrate, bryonia alba root, protortonia cacti, drosera rotundifolia, ipecac, pulsatilla vulgaris, rumex crispus root, pongia officinalis skeleton, roasted, lobaria pulmonaria
Active ingredients: Bryonia alba root — 3 [hp_C]/mLProtortonia cacti — 3 [hp_C]/mLDrosera rotundifolia flowering top — 3 [hp_C]/mLIpecac — 3 [hp_C]/mLPulsatilla vulgaris — 6 [hp_C]/mLRumex crispus root — 6 [hp_C]/mLSpongia officinalis skeleton, Roasted — 3 [hp_C]/mLLobaria pulmonaria — 3 [hp_C]/mLAntimony potassium tartrate — 6 [hp_C]/mL
Dosage form: Syrup
Route: Oral
Labeler: Laboratoires Boiron
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 1, 1993
Listing expires: Dec 31, 2026
Identifiers: Product ID 0220-9032_05173f5f-6763-be69-e063-6394a90a8852SPL ID 05173f5f-6763-be69-e063-6394a90a8852SPL set ID 76589f60-0f09-4d7a-8aaa-f1965df1fe9dUNII T7J046YI2B, LZB7TFX1LT, 75O014T1HG, 62I3C8233L, I76KB35JEV, 9N1RM2S62C, 1PIP394IID, D1YM0P5Z2T, DL6OZ476V3

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

N400220903228 followed by a unit qualifier and the quantity

Package 00220-9032-28. 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 Sep 11, 2023.

Indications (excerpt from the label)

Uses* temporarily relieves dry cough due to minor throat and bronchial irritation as may occur with 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)