Glauco NDC 55714-4810

NDC codes

FDA NDC Directory

Product NDC (as listed)55714-4810Labeler and product segments. Claims need a package NDC.

Product NDC at billing width55714-4810Add 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
55714-4810-1	55714481001	30 mL in 1 BOTTLE, GLASS (55714-4810-1)Marketed from Sep 2, 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): Glauco
Generic name (nonproprietary): aconitum napellus, aurum metallicum, belladonna, causticum, cinchona officinalis, colchicum autumnale, euphrasia officinalis, gelsemium sempervirens, nux vomica, osmium metallicum, phosphorus, physostigma venenosum, rhus toxicodendron, spigelia anthelmia.
Active ingredients: Aconitum napellus — 15 [hp_X]/mLAtropa belladonna — 15 [hp_X]/mLCausticum — 15 [hp_X]/mLCinchona officinalis bark — 15 [hp_X]/mLColchicum autumnale bulb — 15 [hp_X]/mLEuphrasia stricta — 15 [hp_X]/mLGelsemium sempervirens root — 15 [hp_X]/mLStrychnos nux-vomica seed — 15 [hp_X]/mLOsmium — 15 [hp_X]/mLPhosphorus — 15 [hp_X]/mLPhysostigma venenosum seed — 15 [hp_X]/mLToxicodendron pubescens leaf — 15 [hp_X]/mLSpigelia anthelmia — 15 [hp_X]/mLGold — 15 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Newton Laboratories, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 2, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 55714-4810_b5943091-6c09-08d3-e053-2995a90ac912SPL ID b5943091-6c09-08d3-e053-2995a90ac912SPL set ID 9a6394e7-14ed-ced1-e053-2995a90aeb88UNII U0NQ8555JD, WQZ3G9PF0H, DD5FO1WKFU, S003A158SB, 993QHL78E6, C9642I91WL, 639KR60Q1Q, 269XH13919, 2E7M255OPY, 27YLU75U4W, CJV9E9IIOA, 6IO182RP7A, WYT05213GE, 79Y1949PYO
Pharmacologic class: Non-Standardized Plant Allergenic Extract; Standardized Chemical Allergen

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

N455714481001 followed by a unit qualifier and the quantity

Package 55714-4810-01. 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 Dec 3, 2020.

Indications (excerpt from the label)

INDICATIONS & USAGE SECTION Formulated for symptoms such as blurred vision and red eyes..

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)