Baby Mucus Plus Cold Relief NDC 54973-3284

NDC codes

FDA NDC Directory

Product NDC (as listed)54973-3284Labeler and product segments. Claims need a package NDC.

Product NDC at billing width54973-3284Add 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 NDC	11-digit (billing)	Package	Copy
54973-3284-1	54973328401	1 BOTTLE, PLASTIC in 1 CARTON (54973-3284-1) / 118 mL in 1 BOTTLE, PLASTICMarketed from May 13, 2016
54973-3284-3	54973328403	1 BOTTLE, PLASTIC in 1 CARTON (54973-3284-3) / 148 mL in 1 BOTTLE, PLASTICMarketed from Aug 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

Brand name (proprietary): Baby Mucus Plus Cold Relief
Generic name (nonproprietary): bryonia alba root, euphrasia stricta, calcium sulfide, sodium chloride, phosphorus, anemone pulsatilla, rumex crispus root, and silicon dioxide
Active ingredients: Bryonia alba root — 6 [hp_X]/mLEuphrasia stricta — 6 [hp_X]/mLCalcium sulfide — 12 [hp_X]/mLSodium chloride — 30 [hp_X]/mLPhosphorus — 30 [hp_X]/mLAnemone pulsatilla — 6 [hp_X]/mLSilicon dioxide — 12 [hp_X]/mLRumex crispus root — 6 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Hyland's Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 13, 2016
Listing expires: Dec 31, 2026
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)
Identifiers: Product ID 54973-3284_0384ed1c-8da1-f57c-e063-6394a90ad016SPL ID 0384ed1c-8da1-f57c-e063-6394a90ad016SPL set ID d934cc8a-1e43-4942-858a-05b5d068679aUNII T7J046YI2B, C9642I91WL, 1MBW07J51Q, 451W47IQ8X, 27YLU75U4W, I76KB35JEV, ETJ7Z6XBU4, 9N1RM2S62C
Pharmacologic class: Osmotic Laxative

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

N454973328401 followed by a unit qualifier and the quantity

Package 54973-3284-01. 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 Aug 22, 2023.

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)