AllergiClear-M NDC 68703-341

NDC codes

FDA NDC Directory

Product NDC (as listed)68703-341Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68703-0341Add 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
68703-341-02	68703034102	59 mL in 1 BOTTLE, DROPPER (68703-341-02)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): AllergiClear-M
Generic name (nonproprietary): adrenalinum, calcarea fluorica, calcarea phosphorica, euphrasia officinalis, histaminum hydrochloricum, kali muriaticum, natrum muriaticum, silicea
Active ingredients: Calcium phosphate — 8 [hp_X]/59mLCalcium fluoride — 8 [hp_X]/59mLEuphrasia officinalis leaf — 4 [hp_X]/59mLEpinephrine — 7 [hp_C]/59mLHistamine dihydrochloride — 7 [hp_C]/59mLSilicon dioxide — 8 [hp_X]/59mLSodium chloride — 8 [hp_X]/59mLPotassium chloride — 8 [hp_X]/59mL
Dosage form: Liquid
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: Adrenergic alpha-Agonists (Mechanism)Adrenergic beta-Agonists (Mechanism)Calcium (Chemical structure)Catecholamines (Chemical structure)Divalent (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Phosphate Chelating Activity (Mechanism)Potassium Compounds (Chemical structure)
Identifiers: Product ID 68703-341_2ab0f947-8db9-56a7-e063-6394a90ae2eaSPL ID 2ab0f947-8db9-56a7-e063-6394a90ae2eaSPL set ID 9d36096b-022f-5cfa-e053-2995a90a381fUNII 97Z1WI3NDX, O3B55K4YKI, L4W0HL3P0F, YKH834O4BH, 3POA0Q644U, ETJ7Z6XBU4, 451W47IQ8X, 660YQ98I10
Pharmacologic class: Blood Coagulation Factor; Catecholamine; Osmotic Laxative; Phosphate Binder; Potassium Salt; alpha-Adrenergic Agonist; beta-Adrenergic Agonist

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

N468703034102 followed by a unit qualifier and the quantity

Package 68703-0341-02. 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*: Homeopathic medicine for the temporary relief of allergy and hay fever symptoms. *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)