NDC codes

FDA NDC Directory
Product NDC (as listed)71971-6105Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71971-6105Add 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
71971-6105-771971610507719716105071 KIT in 1 KIT (71971-6105-7) * 1 BOTTLE in 1 CARTON (71971-9121-5) / 100 mL in 1 BOTTLE * 1 BOTTLE in 1 CARTON (71971-9151-5) / 100 mL in 1 BOTTLEMarketed from Sep 1, 2022

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
drosera rotundifolia flowering top, arnica montana, bryonia alba whole, ipecacuanha, cetraria islandica subsp. islandica, cochineal, corallium rubrum whole, stannum metallicum, chamomilla, coffea cruda
Dosage form
Kit
Labeler
Homeolab International (Canada) incNDC labeler code 71971
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Identifiers
Product ID 71971-6105_3b271a2a-f5ea-5d80-e063-6394a90a9282SPL ID 3b271a2a-f5ea-5d80-e063-6394a90a9282SPL set ID ab37b0fd-cd18-4823-baef-dedadac86236

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N471971610507 followed by a unit qualifier and the quantity

Package 71971-6105-07. 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 T his ho meo pathic medicine is made from a combination of ingredients traditionally used to help symptoms associated with nighttime cough and cold*; dry cough, cough with expectorantion, chest congestion, aches and pain,fever. *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71971-6105

What is NDC 71971-6105?
71971-6105 is the product NDC for Kids Relief Cough and Cold Syrup Combo Pack Daytime Formula and Nighttime Formula kit, listed with the FDA by Homeolab International (Canada) inc. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Kids Relief Cough and Cold Syrup Combo Pack Daytime Formula and Nighttime Formula (Drosera rotundifolia flowering top, arnica montana, bryonia alba whole, ipecacuanha, cetraria islandica subsp. islandica, cochineal, corallium rubrum whole, stannum metallicum, chamomilla, coffea cruda).
Who is the labeler?
Homeolab International (Canada) inc, NDC labeler code 71971. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Kids Relief Cough and Cold Syrup Combo Pack Daytime Formula and Nighttime Formula?
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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