NDC codes

FDA NDC Directory
Product NDC (as listed)54973-3374Labeler and product segments. Claims need a package NDC.
Product NDC at billing width54973-3374Add 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
54973-3374-154973337401549733374011 KIT in 1 CARTON (54973-3374-1) * 118 mL in 1 BOTTLE, PLASTIC (54973-3284-1) * 118 mL in 1 BOTTLE (54973-3371-2)Marketed from Nov 1, 2018

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)
calcium sulfide,phosphorus,sulfur,rumex crispus root,sodium chloride,arabica coffee bean,anemone pulsatilla,silicon dioxide, goldenseal,onion,bryonia alba root,euphrasia stricta and matricaria chamomilla
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 54973-3374_0397de56-d497-5ac4-e063-6294a90accb2SPL ID 0397de56-d497-5ac4-e063-6294a90accb2SPL set ID 7979fc6f-6d2c-56c9-e053-2991aa0ac1f3

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

N454973337401 followed by a unit qualifier and the quantity

Package 54973-3374-01. 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: ■ accumulation of mucus in chest, throat or nose ■ cough with mucus ■ runny nose ■ sneezing ■ nasal or chest congestion

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 54973-3374

What is NDC 54973-3374?
54973-3374 is the product NDC for Baby Mucus Plus Cold Relief Daytime And Nighttime 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?
Baby Mucus Plus Cold Relief Daytime And Nighttime (Calcium sulfide,phosphorus,sulfur,rumex crispus root,sodium chloride,arabica coffee bean,anemone pulsatilla,silicon dioxide, goldenseal,onion,bryonia alba root,euphrasia stricta and matricaria chamomilla).
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 Baby Mucus Plus Cold Relief Daytime And Nighttime?
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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