What is NDC 66715-9811?

66715-9811 is the product NDC for Zyrtec Allergy, Lil Drug Store, Cetirizine hydrochloride 10 mg/1 tablet, film coated, listed with the FDA by Lil' Drug Store Products, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Zyrtec Allergy, Lil Drug Store (Cetirizine Hydrochloride tablet, film coated).

Lil' Drug Store Products, Inc., NDC labeler code 66715. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Zyrtec Allergy, Lil Drug Store?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Zyrtec Allergy, Lil Drug Store NDC 66715-9811

NDC codes

FDA NDC Directory

Product NDC (as listed)66715-9811Labeler and product segments. Claims need a package NDC.

Product NDC at billing width66715-9811Add 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
66715-9811-1	6671598110166715981101	1 POUCH in 1 CARTON (66715-9811-1) / 1 TABLET, FILM COATED in 1 POUCHMarketed from Jul 10, 2024

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): Zyrtec Allergy, Lil Drug Store
Generic name (nonproprietary): cetirizine hydrochloride tablet, film coated
Active ingredients: Cetirizine hydrochloride — 10 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Lil' Drug Store Products, Inc.NDC labeler code 66715
Product type: Over-the-counter drug
Marketing category: NDA — New Drug ApplicationApplication NDA 019835
Marketing start: Jul 10, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 66715-9811_1b6c945f-5920-8869-e063-6294a90ad397SPL ID 1b6c945f-5920-8869-e063-6294a90ad397SPL set ID 1b6c945f-591f-8869-e063-6294a90ad397RxCUI 1014678, 1020026UNII 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

N466715981101 followed by a unit qualifier and the quantity

Package 66715-9811-01. 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 Jun 21, 2024.

Indications (excerpt from the label)

Uses 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)

About NDC 66715-9811

What is NDC 66715-9811?: 66715-9811 is the product NDC for Zyrtec Allergy, Lil Drug Store, Cetirizine hydrochloride 10 mg/1 tablet, film coated, listed with the FDA by Lil' Drug Store Products, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Zyrtec Allergy, Lil Drug Store (Cetirizine Hydrochloride tablet, film coated).
What is the active ingredient?: Cetirizine hydrochloride.
Who is the labeler?: Lil' Drug Store Products, Inc., NDC labeler code 66715. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Zyrtec Allergy, Lil Drug Store?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other NDCs under NDA 019835

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

FDA NDC Directory listings under NDA 019835
Product	Strength	Form · route	Labeler	Product NDC
Zyrtec Allergycetirizine hydrochloride	Cetirizine hydrochloride 10 mg/1	Tablet, Film coatedOral	Kenvue Brands LLC	50580-726
Zyrtec Allergycetirizine hydrochloride	Cetirizine hydrochloride 5 mg/1	Tablet, Film coatedOral	Kenvue Brands LLC	50580-754
Zyrtec Allergycetirizine hydrochloride	—	Kit	Kenvue Brands LLC	50580-752
Zyrtec Allergycetirizine hydrochloride	Cetirizine hydrochloride 10 mg/1	Tablet, Film coatedOral	RedPharm Drug Inc	67296-1484
Zyrtec Allergycetirizine hydrochloride	Cetirizine hydrochloride 10 mg/1	Tablet, Film coatedOral	Savings Distributors LLC	73097-016
Zyrtec Allergycetirizine hydrochloride	Cetirizine hydrochloride 10 mg/1	Tablet, Film coatedOral	Morning Star OTC	53209-5001
ZYRTEC Hivescetirizine hydrochloride	Cetirizine hydrochloride 10 mg/1	Tablet, Film coatedOral	Kenvue Brands LLC	50580-116
Zyrtec Allergycetirizine hydrochloride	Cetirizine hydrochloride 10 mg/1	Tablet, Film coatedOral	Navajo Manufacturing Company Incorporated	67751-192
Zyrtec Allergycetirizine hydrochloride	Cetirizine hydrochloride 10 mg/1	Tablet, Film coatedOral	Select Consumer Group	85237-2960