NDC codes

FDA NDC Directory
Product NDC (as listed)54973-4113Labeler and product segments. Claims need a package NDC.
Product NDC at billing width54973-4113Add 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
54973-4113-154973411301549734113011 BOTTLE, PLASTIC in 1 CARTON (54973-4113-1) / 118 mL in 1 BOTTLE, PLASTICMarketed from Dec 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)
bryonia alba root,calcium sulfide,pulsatilla vulgaris whole,ferrosoferric phosphate,phosphorus,antimony potassium tartrate,ipecac,rumex crispus root
Active ingredients
Calcium sulfide — 12 [hp_X]/mLPhosphorus — 15 [hp_X]/mLAntimony potassium tartrate — 15 [hp_X]/mLRumex crispus root — 6 [hp_X]/mLFerrosoferric phosphate — 12 [hp_X]/mLPulsatilla vulgaris whole — 12 [hp_X]/mLBryonia alba root — 15 [hp_X]/mLIpecac — 12 [hp_X]/mL
Dosage form
Liquid
Route
Oral
Labeler
Hyland's Consumer Health Inc.NDC labeler code 54973
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Identifiers
Product ID 54973-4113_16c7b1a8-84d8-470b-e063-6394a90a3fbfSPL ID 16c7b1a8-84d8-470b-e063-6394a90a3fbfSPL set ID e72c8fdb-2679-86b3-e053-2a95a90a6cdfUNII 1MBW07J51Q, 27YLU75U4W, DL6OZ476V3, 9N1RM2S62C, 91GQH8I5F7, I76KB35JEV, T7J046YI2B, 62I3C8233L

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

N454973411301 followed by a unit qualifier and the quantity

Package 54973-4113-01. 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 54973-4113

What is NDC 54973-4113?
54973-4113 is the product NDC for Kids Cough and Mucus Daytime Grape Flavor, Calcium sulfide 12 [hp_X]/mL + 7 more ingredients liquid, listed with the FDA by Hyland's Consumer Health 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 Daytime Grape Flavor (Bryonia alba root,Calcium sulfide,Pulsatilla vulgaris whole,Ferrosoferric phosphate,Phosphorus,Antimony potassium tartrate,Ipecac,Rumex crispus root).
What is the active ingredient?
Calcium sulfide, Phosphorus, Antimony potassium tartrate, Rumex crispus root, Ferrosoferric phosphate, Pulsatilla vulgaris whole, Bryonia alba root, Ipecac.
Who is the labeler?
Hyland's Consumer Health 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 Daytime Grape Flavor?
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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