All Day Allergy Relief (cetirizine hcl) NDC 55910-039

NDC codes

FDA NDC Directory

Product NDC (as listed)55910-039Labeler and product segments. Claims need a package NDC.

Product NDC at billing width55910-0039Add 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
55910-039-45	55910003945	1 BOTTLE, PLASTIC in 1 BOX (55910-039-45) / 45 TABLET in 1 BOTTLE, PLASTICMarketed from Jul 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): All Day Allergy Relief
Generic name (nonproprietary): cetirizine hcl
Active ingredients: Cetirizine hydrochloride — 10 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 077946
Marketing start: Jul 1, 2019
Marketing end: Jan 31, 2027
Other FDA classes: Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 55910-039_41bbe91b-7c66-4998-89ab-263654c4fb6dSPL ID 41bbe91b-7c66-4998-89ab-263654c4fb6dSPL set ID 76ec3257-9206-4a0f-a2cf-8a05217b92e7RxCUI 1014678UNII 64O047KTOAUPC 0359726129459
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

N455910003945 followed by a unit qualifier and the quantity

Package 55910-0039-45. 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 Jul 1, 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 077946

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

FDA NDC Directory listings under ANDA 077946
Product	Strength	Form · route	Labeler	Product NDC
Cetirizine Hydrochloride	Cetirizine hydrochloride 10 mg/1	TabletOral	Sandoz Inc	0781-1684