What is NDC 17312-433?

17312-433 is the product NDC for Mucus and Sinus Mucus and Sinus Symptom Relief, Bryonia alba root 15 [hp_X]/mL + 8 more ingredients spray, 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?

Mucus and Sinus Mucus and Sinus Symptom Relief (Bryonia alba, Hydrastis canadensis, Kali bichromicum, Natrum Muriaticum, Pulsatilla pratensis, Silicea, Stannum metallicum, Thuja occidentalis, Zincum gluconicum).

What is the active ingredient?

Bryonia alba root, Zinc gluconate, Thuja occidentalis leafy twig, Tin, Silicon dioxide, Pulsatilla pratensis, Sodium chloride, Potassium dichromate, Goldenseal.

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 Mucus and Sinus Mucus and Sinus Symptom Relief?

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.

NDC 17312-433

NDC codes

FDA NDC Directory

Product NDC (as listed)17312-433Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17312-0433Add 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
17312-433-23	1731204332317312043323	1 BOTTLE, SPRAY in 1 CARTON (17312-433-23) / 20 mL in 1 BOTTLE, SPRAYMarketed from Aug 6, 2024

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): Mucus and Sinus Mucus and Sinus Symptom ReliefSuffix: Mucus and Sinus Symptom Relief
Generic name (nonproprietary): bryonia alba, hydrastis canadensis, kali bichromicum, natrum muriaticum, pulsatilla pratensis, silicea, stannum metallicum, thuja occidentalis, zincum gluconicum
Active ingredients: Bryonia alba root — 15 [hp_X]/mLZinc gluconate — 4 [hp_X]/mLThuja occidentalis leafy twig — 12 [hp_X]/mLTin — 15 [hp_X]/mLSilicon dioxide — 15 [hp_X]/mLPulsatilla pratensis — 12 [hp_X]/mLSodium chloride — 6 [hp_X]/mLPotassium dichromate — 12 [hp_X]/mLGoldenseal — 12 [hp_X]/mL
Dosage form: Spray
Route: Oral
Labeler: TRP CompanyNDC labeler code 17312
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 6, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Decreased Copper Ion Absorption (Physiologic effect)
Identifiers: Product ID 17312-433_46064d86-f228-e9e5-e063-6294a90af1eeSPL ID 46064d86-f228-e9e5-e063-6294a90af1eeSPL set ID 2a42c4a3-9486-9b29-e063-6294a90a7c70UNII T7J046YI2B, U6WSN5SQ1Z, 1NT28V9397, 387GMG9FH5, ETJ7Z6XBU4, 8E272251DI, 451W47IQ8X, T4423S18FM, ZW3Z11D0JV
Pharmacologic class: Copper Absorption Inhibitor

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

N417312043323 followed by a unit qualifier and the quantity

Package 17312-0433-23. 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)

INDICATIONS: Uses* • According to homeopathic indications, these ingredients provide temporary relief from symptoms of mucus and sinus congestion.. *These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 17312-433

What is NDC 17312-433?: 17312-433 is the product NDC for Mucus and Sinus Mucus and Sinus Symptom Relief, Bryonia alba root 15 [hp_X]/mL + 8 more ingredients spray, 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?: Mucus and Sinus Mucus and Sinus Symptom Relief (Bryonia alba, Hydrastis canadensis, Kali bichromicum, Natrum Muriaticum, Pulsatilla pratensis, Silicea, Stannum metallicum, Thuja occidentalis, Zincum gluconicum).
What is the active ingredient?: Bryonia alba root, Zinc gluconate, Thuja occidentalis leafy twig, Tin, Silicon dioxide, Pulsatilla pratensis, Sodium chloride, Potassium dichromate, Goldenseal.
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 Mucus and Sinus Mucus and Sinus Symptom Relief?: 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.

Mucus and Sinus Mucus and Sinus Symptom Relief NDC 17312-433