What is NDC 17312-018?

17312-018 is the product NDC for Bronchial Cough Therapy, Spongia officinalis skeleton, Roasted 6 [hp_C]/1 + 6 more ingredients tablet, orally disintegrating, listed with the FDA by TRP Company. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Bronchial Cough Therapy (Antimony potassium tartrate - protortonia cacti - drosera rotundifolia - echinacea, Unspecified - calcium sulfide - human sputum, Bordetella pertussis infected - spongia officinalis skeleton, Roasted -).

What is the active ingredient?

Spongia officinalis skeleton, Roasted, Antimony potassium tartrate, Protortonia cacti, Drosera rotundifolia, Echinacea, Unspecified, Calcium sulfide, Human sputum, Bordetella pertussis infected.

TRP Company, NDC labeler code 17312. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Bronchial Cough Therapy?

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.

Bronchial Cough Therapy NDC 17312-018 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)17312-018Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17312-0018Add 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
17312-018-14	17312001814	1 BOTTLE in 1 PACKAGE (17312-018-14) / 70 TABLET, ORALLY DISINTEGRATING in 1 BOTTLEMarketed from Dec 1, 2011

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Bronchial Cough Therapy
Generic name (nonproprietary): antimony potassium tartrate - protortonia cacti - drosera rotundifolia - echinacea, unspecified - calcium sulfide - human sputum, bordetella pertussis infected - spongia officinalis skeleton, roasted -
Active ingredients: Spongia officinalis skeleton, Roasted — 6 [hp_C]/1Antimony potassium tartrate — 6 [hp_C]/1Protortonia cacti — 6 [hp_C]/1Drosera rotundifolia — 6 [hp_C]/1Echinacea, Unspecified — 6 [hp_C]/1Calcium sulfide — 6 [hp_C]/1Human sputum, Bordetella pertussis infected — 18 [hp_C]/1
Dosage form: Tablet, Orally disintegrating
Route: Oral
Labeler: TRP CompanyNDC labeler code 17312
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 1, 2011
Listing expires: Dec 31, 2026
Identifiers: Product ID 17312-018_4604e0a2-5b75-5e33-e063-6294a90a6601SPL ID 4604e0a2-5b75-5e33-e063-6294a90a6601SPL set ID f87ad18c-689b-4279-8098-a075ce62bff7UNII 1PIP394IID, DL6OZ476V3, LZB7TFX1LT, QR44N9XPJQ, 4N9P6CC1DX, 1MBW07J51Q, U364V64HUNUPC 0858961001181

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

N417312001814 followed by a unit qualifier and the quantity

Package 17312-0018-14. 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 Dec 15, 2025.

Indications (excerpt from the label)

Uses According to homeopathic indications these ingredients provide temporary relief of symptoms of Bronchial Cough such as: • coughing • mucous build-up • chest tightness and • chest soreness after diagnosis by a physician.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 17312-018

What is NDC 17312-018?: 17312-018 is the product NDC for Bronchial Cough Therapy, Spongia officinalis skeleton, Roasted 6 [hp_C]/1 + 6 more ingredients tablet, orally disintegrating, listed with the FDA by TRP Company. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Bronchial Cough Therapy (Antimony potassium tartrate - protortonia cacti - drosera rotundifolia - echinacea, Unspecified - calcium sulfide - human sputum, Bordetella pertussis infected - spongia officinalis skeleton, Roasted -).
What is the active ingredient?: Spongia officinalis skeleton, Roasted, Antimony potassium tartrate, Protortonia cacti, Drosera rotundifolia, Echinacea, Unspecified, Calcium sulfide, Human sputum, Bordetella pertussis infected.
Who is the labeler?: TRP Company, NDC labeler code 17312. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Bronchial Cough Therapy?: 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.