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
2
Source
full-release
Hydrated at
2026-05-31 23:04:02

Label at a glance#

ProductCVS Pharmacy Coconut Water
Active ingredientBENZALKONIUM CHLORIDE
Label structure6 sections

Dosage and administration

use only to refill a Foaming Hand Soap pump bottle. From pump bottle, apply to dry hands. Work into a rich foamy lather and rinse thoroughly.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

helps eliminate bacteria on hands.

Warnings

WARNINGS SECTION

For external use only

When using this product avoid

OTC - WHEN USING SECTION

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

Stop using this product and ask a doctor if

OTC - STOP USE SECTION

irritation and 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

  • use only to refill a Foaming Hand Soap pump bottle.
  • From pump bottle, apply to dry hands.
  • Work into a rich foamy lather and rinse thoroughly.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Cocamidopropyl Betaine, Polysorbate 20, Fragrance (Parfum), Glycerin, Decyl Glucoside, Hydroxyethylcellulose, Aloe Barbadensis Leaf Juice, Cocos Nucifera (Coconut) Fruit Extract, Bambusa Vulgaris Extract, Propylene Glycol, Polyquaternium-7, Tetrasodium EDTA, Sodium Citrate, Citric Acid, Benzophenone-4, Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1 (CI 42090), Red 33 (CI 17200).

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 SoapPSN2
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD2
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY2
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59779-842-332022-01-28C16284748780-19d75b9d1-12fc-f424-e053-dadaa90a57ceDrug Facts
59779-842-332020-03-18C16284748780-19d75b9d1-12fc-f424-e053-dadaa90a57ceDrug Facts
59779-842-332020-01-31C16284748780-19d75b9d1-12fc-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59779-842-33CVS PharmacyCoconut Water946 mL in 1 BOTTLE, PLASTICLIQUID9462

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59779-842CVS PHARMACY COCONUT WATER (BENZALKONIUM CHLORIDE) LIQUID [CVS PHARMACY]2Legacy NDC, 1 package rows20200319_ad724678-e521-4ad5-b88b-ffb687990fa2.zip

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59779-84259779-842-33

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
POLYSORBATE 207T1F30V5YHIACT
GLYCERINPDC6A3C0OXIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
HYPROMELLOSES3NXW29V3WOIACT
ALOE VERA LEAFZY81Z83H0XIACT
COCONUT3RT3536DHYIACT
BAMBUSA VULGARIS TOPFIW80T6P6VIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW)0L414VCS5YIACT
EDETATE SODIUMMP1J8420LUIACT
SODIUM CITRATE1Q73Q2JULRIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
SULISOBENZONE1W6L629B4KIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
D&C RED NO. 339DBA0SBB0LIACT

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
d2bb745a-fea1-4bd9-8ba0-905f408b6cb7ad724678-e521-4ad5-b88b-ffb687990fa22020-03-18WarningsExact identifier
spl id: d2bb745a-fea1-4bd9-8ba0-905f408b6cb7
spl set id: ad724678-e521-4ad5-b88b-ffb687990fa2

Reported adverse events (FAERS/openFDA)#

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