Amazon Basics All Day Allergy Relief NDC 72288-013

NDC codes

FDA NDC Directory

Product NDC (as listed)72288-013Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72288-0013Add 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
72288-013-40	72288001340	1 BOTTLE in 1 CARTON (72288-013-40) / 40 CAPSULE in 1 BOTTLEMarketed from Aug 26, 2026

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): Amazon Basics All Day Allergy Relief
Generic name (nonproprietary): cetirizine hydrochloride
Active ingredients: Cetirizine hydrochloride — 10 mg/1
Dosage form: Capsule
Route: Oral
Labeler: Amazon.com Services LLC
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 209107
Marketing start: Aug 26, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 72288-013_de313933-f733-4f52-94a4-5273c28f4b1eSPL ID de313933-f733-4f52-94a4-5273c28f4b1eSPL set ID 52163488-0b56-529d-e063-6294a90afc62RxCUI 1014675UNII 64O047KTOA
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

N472288001340 followed by a unit qualifier and the quantity

Package 72288-0013-40. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 209107

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

FDA NDC Directory listings under ANDA 209107
Product	Strength	Form · route	Labeler	Product NDC
Cetirizine Hydrochloride (Allergy)cetirizine hydrochloride	Cetirizine hydrochloride 10 mg/1	CapsuleOral	RITE AID CORPORATION	11822-4228
Cetirizine Hydrochloride (Allergy)cetirizine hydrochloride	Cetirizine hydrochloride 10 mg/1	CapsuleOral	Aurohealth LLC	58602-716
Cetirizine Hydrochloride (Allergy)cetirizine hydrochloride	Cetirizine hydrochloride 10 mg/1	CapsuleOral	Better Living Brands, LLC	21130-099
Cetirizine Hydrochloride (Hives Relief)cetirizine hydrochloride	Cetirizine hydrochloride 10 mg/1	CapsuleOral	Aurohealth LLC	58602-808
Cetirizine Hydrochloride (Allergy)cetirizine hydrochloride	Cetirizine hydrochloride 10 mg/1	CapsuleOral	Aurohealth LLC	58602-806
Cetirizine Hydrochloride (Allergy)cetirizine hydrochloride	Cetirizine hydrochloride 10 mg/1	CapsuleOral	Aurohealth LLC	58602-863
Cetirizine Hydrochloride (Allergy)cetirizine hydrochloride	Cetirizine hydrochloride 10 mg/1	CapsuleOral	WALGREEN CO.	0363-0068