NDC codes

FDA NDC Directory
Product NDC (as listed)54973-3379Labeler and product segments. Claims need a package NDC.
Product NDC at billing width54973-3379Add 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
54973-3379-154973337901549733379011 KIT in 1 CARTON (54973-3379-1) * 1 BOTTLE, PLASTIC in 1 CARTON (54973-3243-1) / 118 mL in 1 BOTTLE, PLASTIC * 1 BOTTLE, PLASTIC in 1 CARTON (54973-3377-1) / 118 mL in 1 BOTTLE, PLASTICMarketed from Dec 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)
onion,anemone pulsatilla, phosphorus, goldenseal, calcium sulfide, sodium chloride, sulfur, matricaria chamomilla and arabica coffee bean
Dosage form
Kit
Route
Oral
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 54973-3379_4651e7fe-6d42-15d9-e063-6394a90a75e2SPL ID 4651e7fe-6d42-15d9-e063-6394a90a75e2SPL set ID 79f26bb5-15ad-e40a-e053-2991aa0aaab3

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

N454973337901 followed by a unit qualifier and the quantity

Package 54973-3379-01. 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 ■ Temporarily relieves symptoms of common cold in children, including: ■ runny nose ■ sore throat ■ sneezing ■ cough ■ post nasal drip ■ nasal or chest congestion

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 54973-3379

What is NDC 54973-3379?
54973-3379 is the product NDC for 4 Kids Cold and Cough Day and Night Grape Flavor 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?
4 Kids Cold and Cough Day and Night Grape Flavor (Onion,anemone pulsatilla, phosphorus, goldenseal, calcium sulfide, sodium chloride, sulfur, matricaria chamomilla and arabica coffee bean).
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 4 Kids Cold and Cough Day and Night Grape Flavor?
1 other product NDC are listed under this name. See all 4 Kids Cold and Cough Day and Night Grape Flavor NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other 4 Kids Cold and Cough Day and Night Grape Flavor NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
4 Kids Cold and Cough Day and Night Grape Flavoronion,anemone pulsatilla, phosphorus, goldenseal, calcium sulfide, sodium chloride, sulfur, matricaria chamomilla and arabica coffee bean—KitOralHyland's Inc.54973-412754973-4127-01

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