All Day Allergy (cetirizine hcl) NDC 41520-212

NDC codes

FDA NDC Directory

Product NDC (as listed)41520-212Labeler and product segments. Claims need a package NDC.

Product NDC at billing width41520-0212Add 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
41520-212-25	41520021225	1 BOTTLE, PLASTIC in 1 BOX (41520-212-25) / 25 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTICMarketed from Dec 31, 2024

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): All Day Allergy
Generic name (nonproprietary): cetirizine hcl
Active ingredients: Cetirizine hydrochloride — 10 mg/1
Dosage form: Capsule, Liquid filled
Route: Oral
Labeler: Care One (American Sales Company)
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 205291
Marketing start: Dec 31, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 41520-212_67a5a75a-7a28-4d07-99b4-8325d1776f3aSPL ID 67a5a75a-7a28-4d07-99b4-8325d1776f3aSPL set ID 01d0729f-11ef-4ec5-8d8e-2863407c3f95RxCUI 1014675UNII 64O047KTOAUPC 0341520001239
Pharmacologic class: Histamine-1 Receptor Antagonist

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

N441520021225 followed by a unit qualifier and the quantity

Package 41520-0212-25. 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 Apr 7, 2025.

Indications (excerpt from the label)

Uses temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose sneezing itchy, watery eyes itching of the nose or throat

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 205291

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 205291
Product	Strength	Form · route	Labeler	Product NDC
Allergy Reliefcetirizine hcl	Cetirizine hydrochloride 10 mg/1	Capsule, Liquid filledOral	WALMART INC. (see also Equate)	79903-344
cetirizine hydrochloride	Cetirizine hydrochloride 10 mg/1	Capsule, Liquid filledOral	Strides Pharma, Inc.	59556-894