FDA.reportPublic FDA data

CVS PHARMACY

Manufacturer
CVS PHARMACY | APOLLO HEALTH AND BEAUTY CARE INC.
Effective date
2020-03-18
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:04:02

Label at a glance#

ProductCVS PHARMACY CITRUS FRESH
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

helps eliminate bacteria on hands

Dosage and administration

apply onto wet hands lather and rinse thoroughly

Storage and handling

store at room temperature

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

helps eliminate bacteria on hands

Warnings

WARNINGS SECTION

For external use only.

When using thhis product

OTC - WHEN USING SECTION

avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or redness develops and lasts.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply onto wet hands
  • lather and rinse thoroughly

Other information

STORAGE AND HANDLING SECTION

store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Cetrimonium Chloride, Glycerin, Lauramidopropylamine Oxide, Sodium Chloride, Cocamide MEA, PEG-120 Methyl Glucose Dioleate, Fragrance (Parfum), Citric Acid, Tetrasodium EDTA, Sodium Sulfate, Citrus Nobilis (Mandarin Orange) Peel Extract, Camellia Sinensis Leaf Extract, Zingiber Officinanle (Ginger) Root Extract, Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1 (CI 42090), Yellow 5 (CI 19140).

Label Copy

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of the labelimage of the label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN4
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD4
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY4
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY4

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
362d7abb-94e6-4c60-9a58-266894157713Product name120231023

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59779-724-562022-01-28C16284748780-19d75b9d0-1930-f424-e053-dadaa90a57ceDRUG FACTS
59779-724-562020-03-18C16284748780-19d75b9d0-1930-f424-e053-dadaa90a57ceDRUG FACTS
59779-724-562020-01-31C16284748780-19d75b9d0-1930-f424-e053-dadaa90a57ceDRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59779-724-56CVS PHARMACYCITRUS FRESH1656 mL in 1 BOTTLE, PLASTICLIQUID16564

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59779-724CVS PHARMACY CITRUS FRESH (BENZALKONIUM CHLORIDE) LIQUID [CVS PHARMACY]4Legacy NDC, 1 package rows20200319_7043c5f1-df5c-4c0f-9156-0de019b506fe.zip

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59779-72459779-724-56

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
FD&C BLUE NO. 1H3R47K3TBDIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
TANGERINE PEELJU3D414057IACT
COCO MONOETHANOLAMIDEC80684146DIACT
GLYCERINPDC6A3C0OXIACT
LAURAMIDOPROPYLAMINE OXIDEI6KX160QTVIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
PEG-120 METHYL GLUCOSE DIOLEATEYM0K64F20VIACT
SODIUM CHLORIDE451W47IQ8XIACT
SODIUM SULFATE0YPR65R21JIACT
EDETATE SODIUMMP1J8420LUIACT
WATER059QF0KO0RIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
GINGERC5529G5JPQIACT

Source Document#

Source XML · Source PDF

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
af1efa36-af41-4e9b-a2ee-549f9bd869707043c5f1-df5c-4c0f-9156-0de019b506fe2020-03-18WarningsExact identifier
spl id: af1efa36-af41-4e9b-a2ee-549f9bd86970
spl set id: 7043c5f1-df5c-4c0f-9156-0de019b506fe

Reported adverse events (FAERS/openFDA)#

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