Mucus Clear Cough and Cold Relief NDC 68703-385

NDC codes

FDA NDC Directory

Product NDC (as listed)68703-385Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68703-0385Add 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
68703-385-02	68703038502	59 mL in 1 BOTTLE, DROPPER (68703-385-02)Marketed from Feb 8, 2023

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): Mucus Clear Cough and Cold Relief
Generic name (nonproprietary): arg met, arsenicum alb, baptisia, brypnia, causticum, dulcamara, echinacea angustifolia, echinacea purp, kali bic, kali mur, merc corros, phos, pulsatilla nutt, senega, zinc pic, zinc val.
Active ingredients: Solanum dulcamara stem — 30 [hp_X]/59mLEchinacea angustifolia — 30 [hp_X]/59mLZinc oxide — 30 [hp_X]/59mLZinc valerate dihydrate — 30 [hp_X]/59mLPhosphorus — 30 [hp_X]/59mLPotassium dichromate — 30 [hp_X]/59mLPotassium chloride — 30 [hp_X]/59mLMercuric chloride — 30 [hp_X]/59mLPulsatilla patens whole — 30 [hp_X]/59mLPolygala senega root — 30 [hp_X]/59mLSilver — 30 [hp_X]/59mLEchinacea purpurea — 30 [hp_X]/59mLBaptisia tinctoria whole — 30 [hp_X]/59mLBryonia alba root — 30 [hp_X]/59mLCausticum — 30 [hp_X]/59mLArsenic trioxide — 30 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: Silver Star Brands
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 8, 2023
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 68703-385_2ab0efa0-68e2-1b30-e063-6294a90ae73eSPL ID 2ab0efa0-68e2-1b30-e063-6294a90ae73eSPL set ID f4378d84-73d5-2170-e053-2a95a90a41c6UNII IR986LE7DF, VB06AV5US8, SOI2LOH54Z, MN0RX54EQA, 27YLU75U4W, T4423S18FM, 660YQ98I10, 53GH7MZT1R, 4M1169RWJD, M7T6H7D4IF, 3M4G523W1G, QI7G114Y98, 5K1UO2888Y, T7J046YI2B, DD5FO1WKFU, S7V92P67HO
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

N468703038502 followed by a unit qualifier and the quantity

Package 68703-0385-02. 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 Jan 1, 2025.

Indications (excerpt from the label)

Uses* Uses*: Temporarily relieves symptoms contributing to congestion, coughs, sneezing, headaches, fever & chills. *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)