CAREALL Allergy Relief

Label at a glance#

Contacts and useful links#

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Loratadine 10mg

OTC - PURPOSE SECTION

Antihistamine

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental overdose, contact a doctor or Poison Control Center right away (1-800-222-1222)

INDICATIONS & USAGE SECTION

Temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

runny nose, itchy/watery eyes, sneezing, itching of the nose or throat

WARNINGS SECTION

Do not useif you have ever had an allergic reaction to this product or any of its ingredients.

Ask a doctor before useif you have liver or kidney disease.  Your doctor should determine if you need a different dose.

When using this productdo not take more than directed.  Taking more than directed may cause drowsiness.

Stop use and ask a doctorif an allergic reaction to this product occurs.  Seek medical help right away.

DOSAGE & ADMINISTRATION SECTION

Adult and children over 6 years old:1 tablets daily: no 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

INACTIVE INGREDIENT SECTION

lactose monohydrate, magnesium stearate, pregelatinized starch, sodium starch glycolate.  

OTHER SAFETY INFORMATION

Store between 20-25 degrees celcius (68-77 degrees farhenheit).

Protect from excessive moisture

Do not use if imprinted seal under bottle cap is broken or missing

You may report side effects 1-888-952-0050

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DailyMed RxNorm Mappings#

Product Linked Resources#

DailyMed Package Descriptions#

DailyMed Billing Units#

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

• CAREALL Allergy Relief
• Loratadine
• MAGNESIUM STEARATE
• SODIUM STARCH GLYCOLATE TYPE A
• LACTOSE MONOHYDRATE
• STARCH, CORN

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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.

Orange Book products#

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

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.

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.

Reported adverse events (FAERS/openFDA)#

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