NDC codes

FDA NDC Directory
Product NDC (as listed)54973-4059Labeler and product segments. Claims need a package NDC.
Product NDC at billing width54973-4059Add 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
54973-4059-154973405901549734059011 KIT in 1 CARTON (54973-4059-1) * 1 BOTTLE, PLASTIC in 1 CARTON (54973-4057-1) / 118 mL in 1 BOTTLE, PLASTIC * 1 BOTTLE, PLASTIC in 1 CARTON (54973-4056-1) / 118 mL in 1 BOTTLE, PLASTICMarketed from Mar 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)
rumex crispus root, antimony potassium tartrate, bryonia alba root, matricaria chamomilla whole, pulsatilla vulgaris, calcium sulfide, ipecac, goldenseal, phosphorus, ferrosoferric phosphate
Dosage form
Kit
Labeler
Hyland's Inc.NDC labeler code 54973
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Identifiers
Product ID 54973-4059_38720b49-2950-dba1-e063-6294a90acedeSPL ID 38720b49-2950-dba1-e063-6294a90acedeSPL set ID d92ab90b-b960-3df2-e053-2a95a90ace89

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

N454973405901 followed by a unit qualifier and the quantity

Package 54973-4059-01. 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 ■ Helps temporarily relieve symptoms of common cold in children, including: ■ cough ■ runny nose ■ sneezing ■ sore throat ■ chest or nasal congestion ■ mucus in chest or throat

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 54973-4059

What is NDC 54973-4059?
54973-4059 is the product NDC for Kids Cough and Mucus Day and Night Grape kit, listed with the FDA by Hyland's Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Kids Cough and Mucus Day and Night Grape (Rumex crispus root, Antimony potassium tartrate, Bryonia alba root, Matricaria chamomilla whole, Pulsatilla vulgaris, Calcium sulfide, Ipecac, Goldenseal, Phosphorus, Ferrosoferric phosphate).
Who is the labeler?
Hyland's Inc., NDC labeler code 54973. 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 Cough and Mucus Day and Night Grape?
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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