Cold NDC 43406-0688

NDC codes

FDA NDC Directory

Product NDC (as listed)43406-0688Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43406-0688Add 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
43406-0688-1	43406068801	30 mL in 1 BOTTLE, DROPPER (43406-0688-1)Marketed from Feb 7, 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): Cold
Generic name (nonproprietary): baptisia tinctoria, echinacea angustifolia, eupatorium perfoliatum, lomatium dissectum, pueraria lobata, trifolium pratense, phytolacca decandra, allium cepa, arsenicum iodatum, baryta carbonica, bromium, calcarea carbonica, kali muriaticum, lachesis mutus, mercurius solubilis, silicea
Active ingredients: Baptisia tinctoria whole — 4 [hp_X]/mLEchinacea angustifolia whole — 4 [hp_X]/mLEupatorium perfoliatum flowering top — 4 [hp_X]/mLLomatium dissectum root — 4 [hp_X]/mLPueraria montana var. Lobata whole — 4 [hp_X]/mLTrifolium pratense flower — 4 [hp_X]/mLPhytolacca americana root — 6 [hp_X]/mLOnion — 12 [hp_X]/mLArsenic triiodide — 12 [hp_X]/mLBarium carbonate — 12 [hp_X]/mLBromine — 12 [hp_X]/mLOyster shell calcium carbonate, Crude — 12 [hp_X]/mLPotassium chloride — 12 [hp_X]/mLLachesis muta venom — 12 [hp_X]/mLMercurius solubilis — 12 [hp_X]/mLSilicon dioxide — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Natural Creations, Inc
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 7, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 43406-0688_b3523678-6826-433e-8ee3-a0a57c07037aSPL ID b3523678-6826-433e-8ee3-a0a57c07037aSPL set ID c45d1d8f-24be-4c13-8c4b-388962421415UNII 5K1UO2888Y, VB06AV5US8, 1W0775VX6E, 5329928G5N, D295OFK7E1, 4JS0838828, 11E6VI8VEG, 492225Q21H, 3029988O2T, 6P669D8HQ8, SBV4XY874G, 2E32821G6I, 660YQ98I10, VSW71SS07I, 324Y4038G2, ETJ7Z6XBU4UPC 0877730000958
Pharmacologic class: Non-Standardized Food Allergenic Extract; Osmotic Laxative; Potassium Salt

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

N443406068801 followed by a unit qualifier and the quantity

Package 43406-0688-01. 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 Nov 20, 2025.

Indications (excerpt from the label)

USES: Temporarily relieves symptoms associated with the common cold.**

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)