What is NDC 54973-3371?

54973-3371 is the product NDC for Baby Nighttime Mucus Plus Cold Relief, Calcium sulfide 12 [hp_X]/mL + 12 more ingredients liquid, 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 Nighttime Mucus Plus Cold Relief (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).

What is the active ingredient?

Calcium sulfide, Phosphorus, Anemone pulsatilla, Silicon dioxide, Goldenseal, Onion, Bryonia alba root, Euphrasia stricta, Matricaria chamomilla, Arabica coffee bean, Sodium chloride, Rumex crispus root, Sulfur.

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 Nighttime Mucus Plus Cold Relief?

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.

Baby Nighttime Mucus Plus Cold Relief NDC 54973-3371

NDC codes

FDA NDC Directory

Product NDC (as listed)54973-3371Labeler and product segments. Claims need a package NDC.

Product NDC at billing width54973-3371Add 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
54973-3371-2	5497333710254973337102	1 BOTTLE, PLASTIC in 1 CARTON (54973-3371-2) / 118 mL in 1 BOTTLE, PLASTICMarketed 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

Brand name (proprietary): Baby Nighttime Mucus Plus Cold Relief
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
Active ingredients: Calcium sulfide — 12 [hp_X]/mLPhosphorus — 30 [hp_X]/mLAnemone pulsatilla — 6 [hp_X]/mLSilicon dioxide — 12 [hp_X]/mLGoldenseal — 6 [hp_X]/mLOnion — 6 [hp_X]/mLBryonia alba root — 6 [hp_X]/mLEuphrasia stricta — 6 [hp_X]/mLMatricaria chamomilla — 3 [hp_X]/mLArabica coffee bean — 3 [hp_X]/mLSodium chloride — 6 [hp_X]/mLRumex crispus root — 6 [hp_X]/mLSulfur — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Hyland's Inc.NDC labeler code 54973
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 1, 2018
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 54973-3371_f98bd339-1709-6f48-e053-6394a90ad617SPL ID f98bd339-1709-6f48-e053-6394a90ad617SPL set ID 736b2487-e81d-d172-e053-2a91aa0ab0cfUNII 1MBW07J51Q, 27YLU75U4W, I76KB35JEV, ETJ7Z6XBU4, ZW3Z11D0JV, 492225Q21H, T7J046YI2B, C9642I91WL, G0R4UBI2ZZ, 3SW678MX72, 451W47IQ8X, 9N1RM2S62C, 70FD1KFU70
Pharmacologic class: Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract

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

N454973337102 followed by a unit qualifier and the quantity

Package 54973-3371-02. 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 Apr 17, 2023.

Indications (excerpt from the label)

Uses ■ Temporarily relieves symptoms of common cold in children at night, including: ■ accumulation of mucus in chest, throat or nose ■ cough with mucus ■ runny nose ■ sneezing ■ nasal or chest congestion ■ occasional sleeplessness

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 54973-3371

What is NDC 54973-3371?: 54973-3371 is the product NDC for Baby Nighttime Mucus Plus Cold Relief, Calcium sulfide 12 [hp_X]/mL + 12 more ingredients liquid, 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 Nighttime Mucus Plus Cold Relief (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).
What is the active ingredient?: Calcium sulfide, Phosphorus, Anemone pulsatilla, Silicon dioxide, Goldenseal, Onion, Bryonia alba root, Euphrasia stricta, Matricaria chamomilla, Arabica coffee bean, Sodium chloride, Rumex crispus root, Sulfur.
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 Nighttime Mucus Plus Cold Relief?: 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.