Allergy Relief

Manufacturer
Bryant Ranch Prepack
Effective date
2019-02-01
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 00:29:10

Label at a glance#

ProductAllergy Relief
Active ingredientCHLORPHENIRAMINE MALEATE
Label structure9 sections

Indications and uses

temporarily relieves these symptoms due to hay fever and other upper respiratory allergies:                 -runny nose                 -sneezing                                -itching of the nose and throat                 -itchy, watery eyes

Dosage and administration

do not exceed recommended dose adults and children 12 years and over: take 1 tablet every 4 to 6 hours, as needed, not more than 6 tablets in 24 hours or as directed by a doctor children under 12 years: consult a doctor

Storage and handling

Tamper Evident: Do not use if imprinted seal under cap is missing or broken. store at room temperature  protect from moisture

Label contents#

Full prescribing information#

Active ingredient (in each tablet)

OTC - ACTIVE INGREDIENT SECTION

Chlorpheniramine maleate 4 mg

Purpose

OTC - PURPOSE SECTION

Antihistamine

Uses

INDICATIONS & USAGE SECTION

  • temporarily relieves these symptoms due to hay fever and other upper respiratory allergies:

                -runny nose

                -sneezing               

                -itching of the nose and throat

                -itchy, watery eyes

Warnings

WARNINGS SECTION

Ask a doctor before use if you have

• glaucoma

• trouble urinating due to an enlarged prostate gland

• a breathing problem such as emphysema or chronic bronchitis

Ask a doctor or pharmacist before use if youare taking sedatives or tranquilizers

When using this product

• drowsiness may occur

• avoid alcoholic drinks

• alcohol, sedatives and tranquilizers may increase drowsiness

• excitability may occur, especially in children

• use caution when driving a motor vehicle or operating machinery.

If pregnant or breast-feeding, ask a health professional before use.


OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • do not exceed recommended dose
  • adults and children 12 years and over: take 1 tablet every 4 to 6
    hours, as needed, not more than 6 tablets in 24 hours or as directed by a doctor
  • children under 12 years: consult a doctor

Other information

STORAGE AND HANDLING SECTION

  • Tamper Evident: Do not use if imprinted seal under cap is missing or broken.
  • store at room temperature 
  • protect from moisture

Inactive ingredients

INACTIVE INGREDIENT SECTION

cellulose, croscarmellose sodium, D and C yellow no. 10 lake, lactose, magnesium stearate, silica, stearic acid.

HOW SUPPLIED

HOW SUPPLIED SECTION

Product: 71335-1015

NDC: 71335-1015-1 30 TABLET in a BOTTLE

NDC: 71335-1015-2 60 TABLET in a BOTTLE

NDC: 71335-1015-3 100 TABLET in a BOTTLE

NDC: 71335-1015-4 120 TABLET in a BOTTLE

NDC: 71335-1015-5 40 TABLET in a BOTTLE

Chlorpheniramine Maleate 4mg Tablet

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label Image
Label Image

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
57896-784-01EA - Each57896-784a1d38e1d-0a63-4d0c-b337-eb04a7b64e5412014-04-03
57896-784-10EA - Each57896-7845163bd9b-d641-4f83-87a1-c50108cd8e5e12018-06-11

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71335-101571335-1015-1, 71335-1015-2, 71335-1015-3, 71335-1015-4, 71335-1015-5
57896-784

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

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
6d005729-843a-4726-a451-6824a3f41910b6afa521-55ea-455b-b43b-2f3c8469d60f2022-03-01WarningsExact identifier
spl set id: b6afa521-55ea-455b-b43b-2f3c8469d60f

Reported adverse events (FAERS/openFDA)#

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