Motion Sickness NDC 55714-2486

NDC codes

FDA NDC Directory

Product NDC (as listed)55714-2486Labeler and product segments. Claims need a package NDC.

Product NDC at billing width55714-2486Add 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
55714-2486-1	55714248601	28 g in 1 BOTTLE, GLASS (55714-2486-1)Marketed from Jan 1, 2019

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): echinacea, hypericum perforatum, passiflora incarnata, valeriana officinalis, absinthium, aconitum napellus, antimonium tartaricum, belladonna, bryonia, carbolicum acidum, colchicum autumnale, conium maculatum, ferrum metallicum, gelsemium sempervirens, glonoinum, hyoscyamus niger, ipecacuanha, iris versicolor, lycopodium clavatum, nux vomica, petroleum, phosphorus, sepia, symphoricarpus racemosus, tabacum, theridion, zingiber officinale.
Active ingredients: Echinacea, Unspecified — 6 [hp_X]/gPassiflora incarnata flowering top — 6 [hp_X]/gValerian — 6 [hp_X]/gWormwood — 15 [hp_X]/gTheridion curassavicum — 15 [hp_X]/gAconitum napellus — 15 [hp_X]/gAntimony potassium tartrate — 15 [hp_X]/gAtropa belladonna — 15 [hp_X]/gBryonia alba root — 15 [hp_X]/gPhenol — 15 [hp_X]/gColchicum autumnale bulb — 15 [hp_X]/gConium maculatum flowering top — 15 [hp_X]/gIron — 15 [hp_X]/gGelsemium sempervirens root — 15 [hp_X]/gNitroglycerin — 15 [hp_X]/gHyoscyamus niger — 15 [hp_X]/gIpecac — 15 [hp_X]/gIris versicolor root — 15 [hp_X]/gLycopodium clavatum spore — 15 [hp_X]/gStrychnos nux-vomica seed — 15 [hp_X]/gKerosene — 15 [hp_X]/gPhosphorus — 15 [hp_X]/gSepia officinalis juice — 15 [hp_X]/gSymphoricarpos albus fruit — 15 [hp_X]/gTobacco leaf — 15 [hp_X]/gHypericum perforatum — 6 [hp_X]/gGinger — 15 [hp_X]/g
Dosage form: Pellet
Route: Oral
Labeler: Newton Laboratories, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 1, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Food Additives (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Nitrates (Chemical structure)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)Vasodilation (Physiologic effect)
Identifiers: Product ID 55714-2486_2d9509a4-abcd-5213-e063-6394a90a827cSPL ID 2d9509a4-abcd-5213-e063-6394a90a827cSPL set ID 9c5a4018-0231-e92b-e053-2995a90a4016UNII 4N9P6CC1DX, CLF5YFS11O, JWF5YAW3QW, F84709P2XV, 9Z8D3HEM8L, U0NQ8555JD, DL6OZ476V3, WQZ3G9PF0H, T7J046YI2B, 339NCG44TV, 993QHL78E6, Q28R5GF371, E1UOL152H7, 639KR60Q1Q, G59M7S0WS3, 4WRK2153H3, 62I3C8233L, X43D4L3DQC, C88X29Y479, 269XH13919, 1C89KKC04E, 27YLU75U4W, QDL83WN8C2, 873JZU3ASZ, 6YR2608RSU, XK4IUX8MNB, C5529G5JPQ
Pharmacologic class: Nitrate Vasodilator; 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

N455714248601 followed by a unit qualifier and the quantity

Package 55714-2486-01. 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 Feb 7, 2025.

Indications (excerpt from the label)

INDICATIONS & USAGE SECTION Formulated for associated symptoms such as the sensation of movement, dizziness, discomfort, headache, nausea and disorientation.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)