What is NDC 11822-2106?

11822-2106 is the product NDC for Rite Aid childrens allergy relief, Cetirizine hydrochloride 1 mg/mL solution, listed with the FDA by Rite Aid Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Rite Aid childrens allergy relief (Cetirizine Hydrochloride).

Rite Aid Corporation, NDC labeler code 11822. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Rite Aid childrens allergy relief?

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.

Rite Aid childrens allergy relief NDC 11822-2106

NDC codes

FDA NDC Directory

Product NDC (as listed)11822-2106Labeler and product segments. Claims need a package NDC.

Product NDC at billing width11822-2106Add 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
11822-2106-8	1182221060811822210608	1 BOTTLE in 1 CARTON (11822-2106-8) / 120 mL in 1 BOTTLEMarketed from May 20, 2011

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): Rite Aid childrens allergy reliefSuffix: childrens allergy relief
Generic name (nonproprietary): cetirizine hydrochloride
Active ingredients: Cetirizine hydrochloride — 1 mg/mL
Dosage form: Solution
Route: Oral
Labeler: Rite Aid CorporationNDC labeler code 11822
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 201546
Marketing start: May 20, 2011
Listing expires: Dec 31, 2027
Other FDA classes: Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 11822-2106_29a12559-c0c3-2b55-e063-6394a90a9255SPL ID 29a12559-c0c3-2b55-e063-6394a90a9255SPL set ID edbefbee-26b6-46bc-abcc-f7b2817705e5RxCUI 1014673UNII 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

N411822210608 followed by a unit qualifier and the quantity

Package 11822-2106-08. 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 Dec 19, 2024.

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)

About NDC 11822-2106

What is NDC 11822-2106?: 11822-2106 is the product NDC for Rite Aid childrens allergy relief, Cetirizine hydrochloride 1 mg/mL solution, listed with the FDA by Rite Aid Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Rite Aid childrens allergy relief (Cetirizine Hydrochloride).
What is the active ingredient?: Cetirizine hydrochloride.
Who is the labeler?: Rite Aid Corporation, NDC labeler code 11822. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Rite Aid childrens allergy relief?: 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 ANDA 201546

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

FDA NDC Directory listings under ANDA 201546
Product	Strength	Form · route	Labeler	Product NDC
All Day Allergycetirizine hydrochloride	Cetirizine hydrochloride 5 mg/5mL	SolutionOral	Amerisource Bergen	46122-101
Allergy Reliefcetirizine hydrochloride	Cetirizine hydrochloride 1 mg/mL	SolutionOral	H E B	37808-106
Cetirizine Hydrochloride	Cetirizine hydrochloride 1 mg/mL	SolutionOral	Sun Pharmaceutical Industries, Inc.	51672-2106
Childrens Allergycetirizine hydrochloride	Cetirizine hydrochloride 1 mg/mL	SolutionOral	Publix Super Markets Inc	56062-106
Childrens Allergy Reliefcetirizine hydrochloride	Cetirizine hydrochloride 5 mg/5mL	SolutionOral	Wal-Mart Stores Inc	49035-106
Childrens Cetirzinecetirizine hydrochloride	Cetirizine hydrochloride 5 mg/5mL	SolutionOral	Pharmacy Value Alliance LLC	68016-106
Wal-Zyr All Day Allergycetirizine hydrochloride	Cetirizine hydrochloride 5 mg/5mL	SolutionOral	WALGREEN COMPANY	0363-2106

Rite Aid childrens allergy relief (Cetirizine hydrochloride) NDC 11822-2106