Over-the-counter drug · ANDA

Allergy Relief (Cetirizine hydrochloride) NDC 21130-712

Cetirizine hydrochloride 10 mg/1 · Tablet · Oral · BETTER LIVING BRANDS, LLC

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 NDC11-digit (billing)PackageCopy
21130-712-03211300712031 BOTTLE in 1 CARTON (21130-712-03) / 30 TABLET in 1 BOTTLEMarketed from May 31, 2023
21130-712-12211300712121 BOTTLE in 1 CARTON (21130-712-12) / 120 TABLET in 1 BOTTLEMarketed from Aug 30, 2023
21130-712-46211300712461 BLISTER PACK in 1 CARTON (21130-712-46) / 14 TABLET in 1 BLISTER PACKMarketed from Jun 26, 2023
21130-712-58211300712581 BOTTLE in 1 CARTON (21130-712-58) / 45 TABLET in 1 BOTTLEMarketed from May 31, 2023
21130-712-81211300712812 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, LLCNDC labeler code 21130
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078933
Marketing start
Listing expires
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 .

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 21130-712

What is NDC 21130-712?
21130-712 is the product NDC for Allergy Relief (cetirizine hydrochloride), Cetirizine hydrochloride 10 mg/1 tablet, listed with the FDA by BETTER LIVING BRANDS, LLC. It has 5 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Allergy Relief (Cetirizine Hydrochloride).
What is the active ingredient?
Cetirizine hydrochloride.
Who is the labeler?
BETTER LIVING BRANDS, LLC, NDC labeler code 21130. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Allergy Relief?
270 other product NDCs are listed under this name. See all Allergy Relief NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Allergy Relief NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Allergy Reliefdiphenhydramine hclDiphenhydramine hydrochloride 25 mg/1Tablet, CoatedOralFamora Inc.87509-000387509-0003-06
Allergy Relieflevocetirizine dihydrochloride usp, 5 mgLevocetirizine dihydrochloride 5 mg/1Tablet, CoatedOralTopco Associates, LLC76162-91576162-0915-3576162-0915-80
Allergy Reliefdiphenhydramine hydrochlorideDiphenhydramine hydrochloride 25 mg/1Tablet, Film coatedOralAmazon.com Services LLC72288-39172288-0391-0172288-0391-78
Allergy Reliefdiphenhydramine hydrochlorideDiphenhydramine hydrochloride 25 mg/1CapsuleOralCARDINAL HEALTH 110, LLC. DBA LEADER70000-077170000-0771-0170000-0771-02
Allergy Relieflevocetirizine dihydrochlorideLevocetirizine dihydrochloride 5 mg/1Tablet, Film coatedOralAmazon.com Services LLC72288-78472288-0784-27
Allergy ReliefloratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralMeijer, Inc.79481-972379481-9723-01
Allergy ReliefloratadineLoratadine 10 mg/1TabletOralDr. Reddy's Laboratories Inc.75907-43475907-0434-0175907-0434-30
Allergy Relieffexofenadine hydrochlorideFexofenadine hydrochloride 180 mg/1Tablet, CoatedOralKroger Company30142-85630142-0856-62
Allergy Relieffexofenadine hydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralNUVICARE LLC84324-04084324-0040-01
Allergy Reliefcetirizine tabletsCetirizine hydrochloride 10 mg/1Tablet, Film coatedOralDISCOUNT DRUG MART, INC53943-13053943-0130-1353943-0130-17

All 271 Allergy Relief NDCs

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
ProductStrengthForm · routeLabelerProduct NDC
All Day Allergy Reliefcetirizine hydrochlorideCetirizine hydrochloride 10 mg/1TabletOralDOLGENCORP, INC.55910-269
Allergycetirizine hydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Film coatedOralKroger Company41226-692
Allergy Reliefcetirizine hydrochlorideCetirizine hydrochloride 10 mg/1TabletOralWALGREENS0363-1794
Cetirizine HydrochlorideCetirizine hydrochloride 5 mg/1TabletOralTIME CAP LABORATORIES, INC.49483-682
Cetirizine Hydrochloride Tablets, 10 mgcetirizine hydrochlorideCetirizine hydrochloride 10 mg/1TabletOralMARKSANS PHARMA LIMITED25000-220
Cetirizine Hydrochloride Tablets, 10 mg (Oval Shape)cetirizine hydrochlorideCetirizine hydrochloride 10 mg/1TabletOralMARKSANS PHARMA LIMITED25000-160
Cetirizine Hydrochloride Tablets, 5 mgcetirizine hydrochlorideCetirizine hydrochloride 5 mg/1TabletOralMARKSANS PHARMA LIMITED25000-219
Cetirizine Hydrochloride Tablets,10 mgcetirizine hydrochlorideCetirizine hydrochloride 10 mg/1TabletOralTIME CAP LABORATORIES, INC.49483-692
Cetirizine Hydrochloride Tablets,10 mgcetirizine hydrochlorideCetirizine hydrochloride 10 mg/1TabletOralNorthwind Health Company, LLC51655-842

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