NDC codes

FDA NDC Directory
Product NDC (as listed)17312-077Labeler and product segments. Claims need a package NDC.
Product NDC at billing width17312-0077Add 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 NDC11-digit (billing)PackageCopy
17312-077-30173120077301 BLISTER PACK in 1 BOX (17312-077-30) / 30 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACKMarketed from May 20, 2020

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

Generic name (nonproprietary)
bryonia, gelsemium sempervirens, sambucus nigra, sulphur, zincum gluconicum
Active ingredients
Bryonia alba root — 6 [hp_X]/1Gelsemium sempervirens root — 6 [hp_X]/1Sambucus nigra flowering top — 3 [hp_X]/1Sulfur — 12 [hp_X]/1Zinc gluconate — 2 [hp_X]/1
Dosage form
Tablet, Orally disintegrating
Route
Oral
Labeler
TRP COMPANYNDC labeler code 17312
Product type
Prescription drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Other FDA classes
Decreased Copper Ion Absorption (Physiologic effect)
Identifiers
Product ID 17312-077_4605009c-3339-197f-e063-6394a90a09c1SPL ID 4605009c-3339-197f-e063-6394a90a09c1SPL set ID a6231fe1-1f0f-04c8-e053-2a95a90a6ee7UNII T7J046YI2B, 639KR60Q1Q, CT03BSA18U, 70FD1KFU70, U6WSN5SQ1ZUPC 0858961001778
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

N417312007730 followed by a unit qualifier and the quantity

Package 17312-0077-30. 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 .

Indications (excerpt from the label)

​Uses* According to homeopathic indications, these ingredients provide temporary relief of cold and flu symptoms such as: • Nasal and sinus congestion, runny nose, sore throat, coughing, sneezing, and chills and fever, after serious causes have been ruled out by a physician. * 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 17312-077

What is NDC 17312-077?
17312-077 is the product NDC for ComPare2 Black Elderberry Cold and Flu Relief, Bryonia alba root 6 [hp_X]/1 + 4 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?
ComPare2 Black Elderberry Cold and Flu Relief (Bryonia, Gelsemium sempervirens, Sambucus nigra, Sulphur, Zincum gluconicum).
What is the active ingredient?
Bryonia alba root, Gelsemium sempervirens root, Sambucus nigra flowering top, Sulfur, Zinc gluconate.
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 ComPare2 Black Elderberry Cold and Flu 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.

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