Allergy Relief (cetirizine hydrochloride) NDC 21130-712

NDC codes

FDA NDC Directory

Product NDC (as listed)21130-712Labeler and product segments. Claims need a package NDC.

Product NDC at billing width21130-0712Add 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
21130-712-03	21130071203	1 BOTTLE in 1 CARTON (21130-712-03) / 30 TABLET in 1 BOTTLEMarketed from May 31, 2023
21130-712-12	21130071212	1 BOTTLE in 1 CARTON (21130-712-12) / 120 TABLET in 1 BOTTLEMarketed from Aug 30, 2023
21130-712-46	21130071246	1 BLISTER PACK in 1 CARTON (21130-712-46) / 14 TABLET in 1 BLISTER PACKMarketed from Jun 26, 2023
21130-712-58	21130071258	1 BOTTLE in 1 CARTON (21130-712-58) / 45 TABLET in 1 BOTTLEMarketed from May 31, 2023
21130-712-81	21130071281	2 BOTTLE in 1 CARTON (21130-712-81) / 90 TABLET in 1 BOTTLE (21130-712-09)Marketed from Jun 23, 2023

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): Allergy Relief
Generic name (nonproprietary): cetirizine hydrochloride
Active ingredients: Cetirizine hydrochloride — 10 mg/1
Dosage form: Tablet
Route: Oral
Labeler: BETTER LIVING BRANDS, LLC
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078933
Marketing start: May 31, 2023
Listing expires: Dec 31, 2026
Other FDA classes: Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 21130-712_38a06b8a-bd81-4696-e063-6294a90a1f38SPL ID 38a06b8a-bd81-4696-e063-6294a90a1f38SPL set ID eb60ae7d-87db-7413-e053-2a95a90afd76RxCUI 1014678UNII 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

N421130071203 followed by a unit qualifier and the quantity

Package 21130-0712-03. 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 Jun 28, 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 078933

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

FDA NDC Directory listings under ANDA 078933
Product	Strength	Form · route	Labeler	Product NDC
Allergy Reliefcetirizine hydrochloride	Cetirizine hydrochloride 10 mg/1	TabletOral	WALGREENS	0363-1794
Cetirizine Hydrochloride Tablets, 10 mg (Oval Shape)cetirizine hydrochloride	Cetirizine hydrochloride 10 mg/1	TabletOral	MARKSANS PHARMA LIMITED	25000-160
Cetirizine Hydrochloride Tablets, 5 mgcetirizine hydrochloride	Cetirizine hydrochloride 5 mg/1	TabletOral	MARKSANS PHARMA LIMITED	25000-219
Cetirizine Hydrochloride Tablets, 10 mgcetirizine hydrochloride	Cetirizine hydrochloride 10 mg/1	TabletOral	MARKSANS PHARMA LIMITED	25000-220
Cetirizine Hydrochloride Tablets,10 mgcetirizine hydrochloride	Cetirizine hydrochloride 10 mg/1	TabletOral	Northwind Health Company, LLC	51655-842
All Day Allergy Reliefcetirizine hydrochloride	Cetirizine hydrochloride 10 mg/1	TabletOral	DOLGENCORP, INC.	55910-269
Allergycetirizine hydrochloride	Cetirizine hydrochloride 10 mg/1	Tablet, Film coatedOral	Kroger Company	41226-692
Cetirizine Hydrochloride	Cetirizine hydrochloride 5 mg/1	TabletOral	TIME CAP LABORATORIES, INC.	49483-682
Cetirizine Hydrochloride Tablets,10 mgcetirizine hydrochloride	Cetirizine hydrochloride 10 mg/1	TabletOral	TIME CAP LABORATORIES, INC.	49483-692