Motion Sickness NDC 54973-9147

NDC codes

FDA NDC Directory

Product NDC (as listed)54973-9147Labeler and product segments. Claims need a package NDC.

Product NDC at billing width54973-9147Add 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
54973-9147-1	54973914701	50 TABLET, SOLUBLE in 1 BOTTLE, PLASTIC (54973-9147-1)Marketed from Dec 1, 1994
54973-9147-2	54973914702	1 BOTTLE, PLASTIC in 1 CARTON (54973-9147-2) / 16 TABLET, SOLUBLE in 1 BOTTLE, PLASTICMarketed from Dec 1, 1994

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): Motion Sickness
Generic name (nonproprietary): strychnos nux-vomica seed, tobacco leaf, kerosene, and anamirta cocculus seed
Active ingredients: Strychnos nux-vomica seed — 6 [hp_X]/1Tobacco leaf — 6 [hp_X]/1Kerosene — 12 [hp_X]/1Anamirta cocculus seed — 30 [hp_X]/1
Dosage form: Tablet, Soluble
Route: Oral
Labeler: Hyland's Consumer Health Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 1, 1994
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 54973-9147_e831b8e5-6f76-bb61-e053-2a95a90a4cc6SPL ID e831b8e5-6f76-bb61-e053-2a95a90a4cc6SPL set ID 13ba963e-94cb-495b-bd1c-8acf214b6f6eUNII 269XH13919, 6YR2608RSU, 1C89KKC04E, 810258W28U
Pharmacologic class: 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

N454973914701 followed by a unit qualifier and the quantity

Package 54973-9147-01. 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 Sep 8, 2022.

Indications (excerpt from the label)

Uses ■ Temporarily relieves symptoms associated with motion sickness, including: ■ nausea ■ headache with nausea ■ vomiting ■ dizziness ■ sour stomach

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)