NDC codes

FDA NDC Directory
Product NDC (as listed)55910-269Labeler and product segments. Claims need a package NDC.
Product NDC at billing width55910-0269Add 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
55910-269-58559100269581 BOTTLE in 1 CARTON (55910-269-58) / 45 TABLET in 1 BOTTLEMarketed from Dec 20, 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)
All Day Allergy Relief
Generic name (nonproprietary)
cetirizine hydrochloride
Active ingredients
Cetirizine hydrochloride — 10 mg/1
Dosage form
Tablet
Route
Oral
Labeler
DOLGENCORP, INC.NDC labeler code 55910
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 55910-269_0c774d83-58dd-d9b3-e063-6394a90a6f7aSPL ID 0c774d83-58dd-d9b3-e063-6394a90a6f7aSPL set ID 0643ea78-9709-8526-e063-6394a90a227bRxCUI 1014678UNII 64O047KTOAUPC 0355910269581
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

N455910026958 followed by a unit qualifier and the quantity

Package 55910-0269-58. 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 55910-269

What is NDC 55910-269?
55910-269 is the product NDC for All Day Allergy Relief (cetirizine hydrochloride), Cetirizine hydrochloride 10 mg/1 tablet, listed with the FDA by DOLGENCORP, INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
All Day Allergy Relief (Cetirizine Hydrochloride).
What is the active ingredient?
Cetirizine hydrochloride.
Who is the labeler?
DOLGENCORP, INC., NDC labeler code 55910. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for All Day Allergy Relief?
14 other product NDCs are listed under this name. See all All Day 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 All Day Allergy Relief NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
All Day Allergy ReliefloratadineLoratadine 10 mg/1TabletOralWALMART INC. (see also Equate)79903-43779903-0437-1279903-0437-36
All Day Allergy ReliefloratadineLoratadine 10 mg/1TabletOralQUALITY CHOICE (Chain Drug Marketing Association)83324-14683324-0146-30
All Day Allergy ReliefloratadineLoratadine 10 mg/1TabletOralQUALITY CHOICE (Chain Drug Marketing Association)83324-14783324-0147-10
All Day Allergy ReliefloratadineLoratadine 10 mg/1TabletOralDolgencorp, Inc. (DOLLAR GENERAL & REXALL)55910-71855910-0718-3055910-0718-60
All Day Allergy ReliefloratadineLoratadine 10 mg/1TabletOralDolgencorp, Inc. (DOLLAR GENERAL & REXALL)55910-98555910-0985-30
All Day Allergy ReliefloratadineLoratadine 10 mg/1TabletOralFamily Dollar (FAMILY WELLNESS)55319-93855319-0938-1055319-0938-30
All Day Allergy ReliefloratadineLoratadine 10 mg/1TabletOralSafeway, Inc.21130-91421130-0914-1021130-0914-1221130-0914-60
All Day Allergy ReliefloratadineLoratadine 10 mg/1TabletOralWALMART INC. (see also Equate)79903-15679903-0156-1079903-0156-1279903-0156-45+2 more
All Day Allergy Reliefcetirizine hclCetirizine hydrochloride 10 mg/1CapsuleOralP & L Development, LLC59726-06459726-0064-12
All Day Allergy Reliefcetirizine hclCetirizine hydrochloride 10 mg/1CapsuleOralP & L Development, LLC59726-74159726-0741-12

All 15 All Day 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
Allergycetirizine hydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Film coatedOralKroger Company41226-692
Allergy Reliefcetirizine hydrochlorideCetirizine hydrochloride 10 mg/1TabletOralWALGREENS0363-1794
Allergy Reliefcetirizine hydrochlorideCetirizine hydrochloride 10 mg/1TabletOralBETTER LIVING BRANDS, LLC21130-712
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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