FDA.reportPublic FDA data

ClorRelief (Chlorpheniramine Maleate 0.5%) Antihistamine Oral Spray

Manufacturer
FERRER MEDICAL INNOVATIONS LLC | Xlear Inc.
Effective date
2026-05-22
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:58:38

Label at a glance#

ProductClorRelief
Active ingredientCHLORPHENIRAMINE MALEATE
Label structure7 sections

Indications and uses

Temporarily relieves symptoms of hay fever or other upper respiratory allergies: runny nose itchy nose or throat sneezing itchy, watery eyes

Dosage and administration

Adults and children 12 years and over: For each application, spray 4 times every 4 to 6 hours, do not exceed 6 applications in 24 hours. Children 6 to under 12 years of age: Should be supervised in the use of this product. For each application, spray 2 times every 4 to 6 hours. Do not exceed 3 applications in 24 hours. Children 4 to under 6 years of age: Do not use unless directed by a doctor. Children under 4 yea...

Storage and handling

Store at room temperature 15-30° C (59-86° F)

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Chlorpheniramine Maleate 0.5%

Purpose

OTC - PURPOSE SECTION

Antihistamine

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves symptoms of hay fever or other upper respiratory allergies:

  • runny nose
  • itchy nose or throat
  • sneezing itchy, watery eyes

Warnings

WARNINGS SECTION

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

glaucoma a breathing problem such as emphysema or chronic bronchitis trouble urinating due to an enlarged prostate gland

Ask a doctor or pharmacist before use if

OTC - ASK DOCTOR/PHARMACIST SECTION

you are taking sedatives or tranquilizers

When using this product

OTC - WHEN USING SECTION

  • you may get drowsy
  • avoid alcoholic drinks, sedatives & tranquilizers, may increase drowsiness
  • be careful when driving a motor vehicle or operating machinery
  • excitability may occur, especially in children

If pregnant or breastfeeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask your doctor before use.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Do not use to make a child sleepy. In case of overdose, getmedical help or contact a Poison Control Center right away.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Vera, glycerin, grapefruit seed extract, hyaluronic acid, peppermint flavor, purified water, stevia, xylitol.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years and over:

For each application, spray 4 times every 4 to 6 hours,

do not exceed 6 applications in 24 hours.

Children 6 to under 12 years of age:
Should be supervised in the use of this product. For each application, spray 2 times every 4 to 6 hours. Do not exceed 3 applications in 24 hours.

Children 4 to under 6 years of age:
Do not use unless directed by a doctor.

Children under 4 years of age:
Do not use.

Other Information

STORAGE AND HANDLING SECTION

Store at room temperature 15-30° C (59-86° F)

ClorRelief Box

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ClorRelief Carton OutlineClorRelief Carton Outline

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2610305chlorpheniramine maleate 0.5 % Mucosal SprayPSN4
2610310ClorRelief 0.5 % Mucosal SprayPSN4
2610310chlorpheniramine maleate 5 MG/ML Mucosal Spray [Clorrelief]SBD4
2610305chlorpheniramine maleate 5 MG/ML Mucosal SpraySCD4
2610305chlorpheniramine maleate 0.5 % Mucosal SpraySY4
2610310ClorRelief 0.5 % Mucosal SpraySY4
2610310Clorrelief 5 MG/ML Mucosal SpraySY4

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CHLORPHENIRAMINE Pharmacologic Class Indexing3Indexing - Pharmacologic Class20180813

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codeqrco.de/bdROHPClorRelief Outline.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d17a97fa-387f-690e-d2be-0083ab044a03Product name320170725
0fdb98e2-b951-a1ce-5715-2b187ba500efProduct name420170718
c6fba691-a132-4ede-95c6-f8c6bd696636Product name120150902
c0200ab5-4954-454e-9676-30b741b245bdProduct name120150730

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82643-002-152025-01-30C16284748780-12cef2736-720d-d83d-e063-dadaa90ab31fClorRelief (Chlorpheniramine Maleate 0.5%) Antihistamine Oral Spray

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82643-002-15ClorRelief15 mL in 1 BOTTLE, WITH APPLICATORAEROSOL, SPRAY154
82643-002-15ClorRelief1 in 1 CARTONAEROSOL, SPRAY14

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82643-00282643-002-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
XYLITOLVCQ006KQ1EIACT
WATER059QF0KO0RIACT
CHLORPHENIRAMINE MALEATEV1Q0O9OJ9ZACTIB
GLYCERINPDC6A3C0OXIACT
ALOE VERA WHOLEKIZ4X2EHYXIACT
PEPPERMINTV95R5KMY2BIACT
GRAPEFRUIT SEED OIL598D944HOLIACT
HYALURONIC ACIDS270N0TRQYIACT
STEVIA LEAF6TC6NN0876IACT

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
ClorReliefCHLORPHENIRAMINE MALEATEFERRER MEDICAL INNOVATIONS LLCdb729011-f72f-5911-e053-2a95a90a68bf2026-05-22WarningsExact identifier
ndc (package): 82643-002-15
ndc (product): 82643-002
ndc11 (package): 82643000215
spl id: 526f9c82-d393-f544-e063-6394a90a29d9
spl set id: db729011-f72f-5911-e053-2a95a90a68bf

Reported adverse events (FAERS/openFDA)#

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