Mucus-Clear Flu Relief NDC 68703-369

NDC codes

FDA NDC Directory

Product NDC (as listed)68703-369Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68703-0369Add 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
68703-369-59	68703036959	59 mL in 1 BOTTLE, GLASS (68703-369-59)Marketed from Sep 7, 2021

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 Flu Relief
Generic name (nonproprietary): anas barbariae, arsenicum alb, baptisia, echinacea purp, gelsemium, influenzinum, phytolacca, sarcolacticum ac, sulphur, zinc acet, zinc mur, zinc oxy
Active ingredients: Arsenic trioxide — 60 [hp_X]/59mLBaptisia tinctoria — 60 [hp_X]/59mLEchinacea purpurea — 60 [hp_X]/59mLGelsemium sempervirens root — 60 [hp_X]/59mLLactic acid, L- — 60 [hp_X]/59mLZinc acetate — 60 [hp_X]/59mLCairina moschata heart/liver autolysate — 60 [hp_X]/59mLInfluenza a virus whole — 60 [hp_X]/59mLZinc chloride — 60 [hp_X]/59mLInfluenza b virus whole — 60 [hp_X]/59mLPhytolacca americana root — 60 [hp_X]/59mLSulfur — 60 [hp_X]/59mLZinc oxide — 60 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: Silver Star Brands
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 7, 2021
Listing expires: Dec 31, 2026
Other FDA classes: Decreased Copper Ion Absorption (Physiologic effect)Decreased Copper Ion Absorption (Physiologic effect)
Identifiers: Product ID 68703-369_2ab10b12-68e1-3af8-e063-6294a90af21fSPL ID 2ab10b12-68e1-3af8-e063-6294a90af21fSPL set ID c442a928-4745-40d9-e053-2a95a90ad36cUNII S7V92P67HO, 5K1UO2888Y, QI7G114Y98, 639KR60Q1Q, F9S9FFU82N, FM5526K07A, RN2HC612GY, R9HH0NDE2E, 86Q357L16B, 1314JZ2X6W, 11E6VI8VEG, 70FD1KFU70, SOI2LOH54ZUPC 0818837013960
Pharmacologic class: Copper Absorption Inhibitor

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

N468703036959 followed by a unit qualifier and the quantity

Package 68703-0369-59. 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 fatigue, headaches, body aches, fever, chills nausea, vomiting and diarrhea. Uses:* Temporarily relieves fatigue, headaches, body aches, fever, chills, nausea, vomiting and diarrhea. *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)