CVS PHARMACY

Manufacturer
CVS PHARMACY | APOLLO HEALTH AND BEAUTY CARE
Effective date
2014-02-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:38:30

Key Label Information#

Active Ingredients And Purpose

ACTIVE INGREDIENT

BENZALKONIUM CHLORIDE 0.13%

Uses

USES

HELPS ELIMINATE BACTERIA ON HANDS

Warnings

WARNINGS

FOR EXTERNAL USE ONLY

Directions And Dosage

DIRECTIONS

APPLY ONTO WET HANDS. WORK INTO LATHER, RINSE AND DRY THOROUGHLY

Other Label Information

OTHER INFORMATION

STORE AT ROOM TEMPERATURE

INACTIVE INGREDIENTS

WATER (AQUA), COCAMIDOPROPYL BETAINE, HYDROXYETHYLCELLULOSE, GLYCERIN, DECYL GLUCOSIDE, ALOE BARBADENSIS LEAF JUICE, FRAGRANCE (PARFUM), POLYQUATERNIUM-7, POLOXAMER 124, TETRASODIUM EDTA, SODIUM CITRATE, CITRIC ACID, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, BLUE 1 (CI 42090), EXT. VIOLET 2 (CI 60730)

LABEL COPY

Label Images#

13954L
13954L

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN1
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD1
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY1
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59779-723-102020-01-31C16284748780-19d75b9d0-a330-f424-e053-dadaa90a57ceDRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59779-723-10CVS PHARMACYFRESH WATER295 mL in 1 BOTTLE, PLASTICLIQUID2951

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59779-723CVS PHARMACY FRESH WATER (BENZALKONIUM CHLORIDE) LIQUID [CVS PHARMACY]1Legacy NDC, 1 package rows20140226_99e1f103-df3d-46cd-bc0e-e24f032aa7af.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
BENZALKONIUM CHLORIDEACTIVE INGREDIENTF5UM2KM3W71
BENZALKONIUMACTIVE MOIETY7N6JUD5X6Y1
ALOE VERA LEAFINACTIVE INGREDIENTZY81Z83H0X1
CITRIC ACID MONOHYDRATEINACTIVE INGREDIENT2968PHW8QP1
COCAMIDOPROPYL BETAINEINACTIVE INGREDIENT5OCF3O11KX1
DECYL GLUCOSIDEINACTIVE INGREDIENTZ17H97EA6Y1
EDETATE SODIUMINACTIVE INGREDIENTMP1J8420LU1
EXT. D&C VIOLET NO. 2INACTIVE INGREDIENTG5UX3K07281
FD&C BLUE NO. 1INACTIVE INGREDIENTH3R47K3TBD1
GLYCERININACTIVE INGREDIENTPDC6A3C0OX1
HYDROXYETHYL CELLULOSE (5000 CPS AT 1%)INACTIVE INGREDIENTX70SE62ZAR1
METHYLCHLOROISOTHIAZOLINONEINACTIVE INGREDIENTDEL7T5QRPN1
METHYLISOTHIAZOLINONEINACTIVE INGREDIENT229D0E1QFA1
POLOXAMER 124INACTIVE INGREDIENT1S66E28KXA1
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW)INACTIVE INGREDIENT0L414VCS5Y1
SODIUM CITRATEINACTIVE INGREDIENT1Q73Q2JULR1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59779-72359779-723-10

Ingredients#

Complete SPL Sections#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

BENZALKONIUM CHLORIDE 0.13%

USES

INDICATIONS & USAGE SECTION

HELPS ELIMINATE BACTERIA ON HANDS

WARNINGS

WARNINGS SECTION

FOR EXTERNAL USE ONLY

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

APPLY ONTO WET HANDS. WORK INTO LATHER, RINSE AND DRY THOROUGHLY

OTHER INFORMATION

STORAGE AND HANDLING SECTION

STORE AT ROOM TEMPERATURE

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

WATER (AQUA), COCAMIDOPROPYL BETAINE, HYDROXYETHYLCELLULOSE, GLYCERIN, DECYL GLUCOSIDE, ALOE BARBADENSIS LEAF JUICE, FRAGRANCE (PARFUM), POLYQUATERNIUM-7, POLOXAMER 124, TETRASODIUM EDTA, SODIUM CITRATE, CITRIC ACID, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, BLUE 1 (CI 42090), EXT. VIOLET 2 (CI 60730)

LABEL COPY

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Source Document#

Source XML