Loratadine Orally Disintegrating Tablets USP 10 mg

Manufacturer
Ahold U.S.A., Inc, | Aurohealth LLC | Aurobindo Pharma Limited
Effective date
2022-11-04
Label type
Human OTC Drug Label
Version
4
Source
full-release
Hydrated at
2026-05-31 23:51:22

Label at a glance#

ProductLoratadine ODT
Active ingredientLORATADINE
Label structure14 sections

Indications and 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

Dosage and administration

place 1 tablet on tongue; tablet disintegrates, with or without water   adults and children 6 years and over  1 tablet daily; not more than 1 tablet in 24 hours  children under 6 years of age  ask a doctor  consumers with liver or kidney disease  ask a doctor

Storage and handling

Phenylketonurics: Contains phenylalanine 2.25 mg per tablet do not use if the individual blister unit is open or torn store at 20° to 25°C (68° to 77°F) use tablet immediately after opening individual blister Complies with USP test 2 for Disintegration

Label contents#

Full prescribing information#

Active ingredient (in each tablet)

OTC - ACTIVE INGREDIENT SECTION

Loratadine USP 10 mg

Purpose

OTC - PURPOSE SECTION

Antihistamine

Uses

INDICATIONS & USAGE SECTION

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

Do not use

OTC - DO NOT USE SECTION

if you have ever had an allergic reaction to this product or any of its ingredients.

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

liver or kidney disease. Your doctor should determine if you need a different dose.

When using this product

OTC - WHEN USING SECTION

do not take more than directed. Taking more than directed may cause drowsiness.

Stop use and ask a doctor if

OTC - STOP USE SECTION

an allergic reaction to this product occurs. Seek medical help right away.

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION


  • place 1 tablet on tongue; tablet disintegrates, with or without water 

 adults and children 6 years and over
 1 tablet daily; not more than 1 tablet in 24 hours
 children under 6 years of age
 ask a doctor
 consumers with liver or kidney disease
 ask a doctor

Other information

STORAGE AND HANDLING SECTION

  • Phenylketonurics: Contains phenylalanine 2.25 mg per tablet
  • do not use if the individual blister unit is open or torn
  • store at 20° to 25°C (68° to 77°F)
  • use tablet immediately after opening individual blister
  • Complies with USP test 2 for Disintegration

Inactive ingredients

INACTIVE INGREDIENT SECTION

aspartame, crospovidone, mannitol, microcrystalline cellulose,  peppermint, pregelatinized starch (maize), sodium stearyl fumarate

Questions or comments?

OTC - QUESTIONS SECTION

call 1-855-274-4122

Distributed By
FOODHOLD U.S.A., LLC
LANDOVER, MD 20785
1-877-846-9949
©2018 S&S Brands, LLC

Made in India
Quality guaranteed
or your money back.
Code: TS/DRUGS/22/2009

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 10 mg, Blister Carton 10 (1 X 10) Orally Disintegrating Tablets

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CAREONE®
NDC 60000-950-83

Compare to the active ingredient
in Claritin®  RediTabs®†
 
24 hr

Original Prescription Strength
Non-Drowsy*

Allergy Relief

Loratadine Orally Disintegrating
Tablets USP 100 mg

No water needed,
melts in your mouth

Actual Size

10 Orally Disintegrating Tablets

Indoor & Outdoor Allergies

Relief of:

  • Sneezing
  • Runny Nose
  • Itchy, Water Eyes
  • Itchy Throat or Nose

No Water Needed
Melts in Your Mouth
*When taken as directed.
See Drug Facts Panel. 

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 10 mg, Blister Carton 10 (1 X 10) Orally Disintegrating TabletsPACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 10 mg, Blister Carton 10 (1 X 10) Orally Disintegrating Tablets








DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
311373loratadine 10 MG 24HR Disintegrating Oral TabletPSN4
311373loratadine 10 MG Disintegrating Oral TabletSCD4

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
a62a50ac-1535-4461-9768-8ae703e2e9fbProduct name120210525
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877Product name120140508
bc07ef78-e82d-0c19-31f4-31f263780582Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60000-950-83Loratadine ODT10 in 1 BLISTER PACKTABLET, ORALLY DISINTEGRATING104
60000-950-83Loratadine ODT1 in 1 CARTONTABLET, ORALLY DISINTEGRATING14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60000-950LORATADINE ODT (LORATADINE) TABLET, ORALLY DISINTEGRATING [AHOLD U.S.A., INC,]4Current NDC, Legacy NDC, 2 package rows20221105_092aec8d-57d5-4487-8e1a-b4b586bee7cf.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60000-95060000-950-83

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

Orange Book application contexts#

All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.

Orange Book application contexts page 1 of 1 · 1 matching rows.

Source provenance: Browse the complete Orange Book source catalog · source snapshot 43.

Orange Book products#

Current product rows page 1 of 1 · 1 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A208477-001LORATADINELORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-11

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Product history page 1 of 2 · 43 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-09-14 22:38:342026-08A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-1184e616aacf4f…
2026-08-18 06:07:402026-07A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-11caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-11011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-1131067a03dcf5…
2025-08-23 18:47 UTC2025-08A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-116a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-11fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-11b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-1103ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-112680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-115bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-11d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-11d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-1179d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-11301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-111e350fbaab3a…
2024-05-31 18:47 UTC2024-05A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-118072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-115c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-115d02ea3f76ae…
2022-04-04 05:41 UTC2022-04A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-114b0b4de00fa7…
2019-12-13 00:20 UTC2019-12A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-1174a2ff9319b5…
2022-03-09 01:35 UTC2022-03A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-11bb7c543d1eb4…
2021-12-28 21:50 UTC2021-12A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-11782e0a99824c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-1187673890dc5c…
2021-03-12 10:30 UTC2021-03A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-115aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-118869cabd3fbd…
2020-11-12 02:37 UTC2020-11A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-11c0c555d07b60…
2019-12-14 00:12 UTC2019-12A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-113f01610625f2…
2019-09-15 20:21 UTC2019-09A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-11b00525d2431f…
2019-07-19 19:46 UTC2019-07A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-11ea99ee380514…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-116a51e52b5d6a…
2024-02-18 07:12 UTC2024-02A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-111c564ffb4f44…
2023-12-20 04:57 UTC2023-12A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-11ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-11a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-119b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-11a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-113f0d92c62455…
2023-05-13 08:27 UTC2023-05A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-11053a50430f4f…
2023-01-26 05:58 UTC2023-01A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-113bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-113a93d1ddd44b…
2022-10-28 04:53 UTC2022-10A208477-001LORATADINE10MGTABLET, ORALLY DISINTEGRATING / ORAL2018-04-11f41ea6bd6efb…

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Loratadine ODTLORATADINEAhold U.S.A., Inc,092aec8d-57d5-4487-8e1a-b4b586bee7cf2022-11-04WarningsExact identifier
ndc (package): 60000-950-83
ndc (product): 60000-950
ndc11 (package): 60000095083
spl id: d84e29dc-9c76-4b9c-a260-9d04c5f83bc1
spl set id: 092aec8d-57d5-4487-8e1a-b4b586bee7cf

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.