Allergy NDC 81825-0007

NDC codes

FDA NDC Directory

Product NDC (as listed)81825-0007Labeler and product segments. Claims need a package NDC.

Product NDC at billing width81825-0007Add 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
81825-0007-1	81825000701	30 mL in 1 BOTTLE, DROPPER (81825-0007-1)Marketed from Feb 16, 2022

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): Allergy
Generic name (nonproprietary): allium cepa, ambrosia, arsenicum alb, carbo veg, euphrasia, nux vom, phosphorus, pulsatilla, sulphur, solidago
Active ingredients: Onion — 30 [hp_C]/mLAmbrosia artemisiifolia whole — 30 [hp_C]/mLActivated charcoal — 30 [hp_C]/mLEuphrasia stricta — 30 [hp_C]/mLStrychnos nux-vomica seed — 30 [hp_C]/mLPhosphorus — 30 [hp_C]/mLPulsatilla vulgaris whole — 30 [hp_C]/mLSulfur — 30 [hp_C]/mLSolidago virgaurea flowering top — 30 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Zorex International
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 16, 2022
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 81825-0007_dda1ff79-ce5d-47c0-99e6-0b77f3defed7SPL ID dda1ff79-ce5d-47c0-99e6-0b77f3defed7SPL set ID 4718c012-b90d-4d7a-a97c-1abec1fd3834UNII 492225Q21H, 9W34L2CQ9A, 2P3VWU3H10, C9642I91WL, 269XH13919, 27YLU75U4W, I76KB35JEV, 70FD1KFU70, 5405K23S50UPC 0713289148089
Pharmacologic class: Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract

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

N481825000701 followed by a unit qualifier and the quantity

Package 81825-0007-01. 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 21, 2018.

Indications (excerpt from the label)

USES: Temporarily relieves hay fever, coryza, itching and burning eyes, coughing and/or other symptoms associated with hay fever and allergies.**

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)