Cough and Cold Relief NDC 68703-345

NDC codes

FDA NDC Directory

Product NDC (as listed)68703-345Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68703-0345Add 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
68703-345-02	68703034502	59 mL in 1 BOTTLE, SPRAY (68703-345-02)Marketed from Oct 1, 2019

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Cough and Cold Relief
Generic name (nonproprietary): arg met, arsenicum alb, baptisia, bryonia, causticum, dulcamara, echinacea angustifolia, echinacea purp, kali bic, merc coros, phos, pulsatilla nutt, senega, zinc pic, zinc val
Active ingredients: Phosphorus — 10 [hp_X]/59mLZinc picrate — 10 [hp_X]/59mLPolygala senega root — 10 [hp_X]/59mLZinc valerate — 10 [hp_X]/59mLMercuric chloride — 10 [hp_X]/59mLArsenic trioxide — 10 [hp_X]/59mLPotassium dichromate — 10 [hp_X]/59mLBaptisia tinctoria — 10 [hp_X]/59mLCausticum — 10 [hp_X]/59mLEchinacea purpurea — 10 [hp_X]/59mLAnemone patens whole — 10 [hp_X]/59mLEchinacea angustifolia — 10 [hp_X]/59mLPotassium chloride — 10 [hp_X]/59mLSilver — 10 [hp_X]/59mLSolanum dulcamara flower — 10 [hp_X]/59mL
Dosage form: Spray
Route: Oral
Labeler: Silver Star Brands
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 1, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)
Identifiers: Product ID 68703-345_28687e60-9781-0d43-e063-6394a90a03e9SPL ID 28687e60-9781-0d43-e063-6394a90a03e9SPL set ID 9d4a851c-ebda-1918-e053-2995a90a4936UNII 27YLU75U4W, 9JNG88GK4F, M7T6H7D4IF, HHJ036TQR0, 53GH7MZT1R, S7V92P67HO, T4423S18FM, 5K1UO2888Y, DD5FO1WKFU, QI7G114Y98, 4M1169RWJD, VB06AV5US8, 660YQ98I10, 3M4G523W1G, W6J1279A6KUPC 0818837015292
Pharmacologic class: 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

N468703034502 followed by a unit qualifier and the quantity

Package 68703-0345-02. 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 Dec 3, 2024.

Indications (excerpt from the label)

Uses* Temporarily relieves symptoms contributing to congestion, coughs, sneezing, headaches, fever & chills. *This statement has not been evaluated by the Food and drug Administration. This product is not intended to diagnose, treat, cure or prevent any disease.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)