Kids Cold and Cough Nighttime Grape Flavor NDC 54973-4111

NDC codes

FDA NDC Directory

Product NDC (as listed)54973-4111Labeler and product segments. Claims need a package NDC.

Product NDC at billing width54973-4111Add 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
54973-4111-1	54973411101	1 BOTTLE, PLASTIC in 1 CARTON (54973-4111-1) / 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

Brand name (proprietary): Kids Cold and Cough Nighttime Grape Flavor
Generic name (nonproprietary): onion, chamomile, arabica coffee bean, calcium sulfide, golden seal, sodium chloride, phosphorus, pulsatilla vulgaris top, sulfur
Active ingredients: Calcium sulfide — 12 [hp_X]/mLGoldenseal — 6 [hp_X]/mLChamomile — 6 [hp_X]/mLSodium chloride — 6 [hp_X]/mLOnion — 6 [hp_X]/mLArabica coffee bean — 6 [hp_X]/mLPulsatilla vulgaris top — 6 [hp_X]/mLSulfur — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Hyland's Consumer Health Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 1, 2022
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 54973-4111_e676dbb7-2130-47e3-e053-2995a90af4e1SPL ID e676dbb7-2130-47e3-e053-2995a90af4e1SPL set ID e676dbb7-212f-47e3-e053-2995a90af4e1UNII 1MBW07J51Q, ZW3Z11D0JV, FGL3685T2X, 451W47IQ8X, 492225Q21H, 3SW678MX72, 4F1D271XW0, 70FD1KFU70, 27YLU75U4W
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

N454973411101 followed by a unit qualifier and the quantity

Package 54973-4111-01. 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 17, 2022.

Indications (excerpt from the label)

Uses ■ Helps temporarily relieve symptoms of common cold in children at night, including: ■ cough ■ runny nose ■ post nasal drip ■ sneezing ■ sore throat ■ nasal or chest congestion ■ occasional sleeplessness

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)