FDA.reportPublic FDA data

NDC- 51316-706

Manufacturer
CVS PHARMACY, INC | Apollo Health and Beauty Care
Effective date
2026-05-02
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:56:26

Label at a glance#

ProductHandsoap
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride

OTC - PURPOSE SECTION

Hand washing

WARNINGS SECTION

OTC - WHEN USING SECTION

OTC - STOP USE SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Incase of accidental ingestion, get medical help or contact poison control centre immediately.

DOSAGE & ADMINISTRATION SECTION

Apply onto dry hands, work into a lather, rinse and dry throughly.

INACTIVE INGREDIENT SECTION

Water( Aqua), Cocamidopropyl Betaine, Polysorbate 20, Fragrance (Parfum), Glycerin, Decyl Glucoside, Hydroxyethylcellulose, Aloe Barbadensis, Camellia Sinensis Leaf Extract,Polyquaternium-7, Tetrasodium EDTA, Sodium Citrate, Citric Acid, Benzophenone -4, Methylcholoroisothiazolinone, Methylisothiazolinone, Yellow 10 (Cl 47005), Green 3 (Cl 42053)

INDICATIONS & USAGE SECTION

Helps eliminate bacteria on the skin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDP -1 PEARPDP -1 PEAR

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 Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51316-706-07Handsoap222 mL in 1 BOTTLE, PLASTICSOAP2224

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51316-70651316-706-07

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
D&C YELLOW NO. 1035SW5USQ3GIACT
FD&C GREEN NO. 33P3ONR6O1SIACT
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD)0L414VCS5YIACT
SODIUM CITRATE1Q73Q2JULRIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
POLYSORBATE 207T1F30V5YHIACT
FRAGRANCE CLEAN ORC0600327329LCV5BTFIACT
GLYCERINPDC6A3C0OXIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%)S38J6RZN16IACT
GREEN TEA LEAFW2ZU1RY8B0IACT
SULISOBENZONE1W6L629B4KIACT
EDETATE SODIUMMP1J8420LUIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
HandsoapBENZALKONIUM CHLORIDECVS PHARMACY, INCe584a181-1226-5dda-e053-2a95a90ab6452026-05-02WarningsExact identifier
ndc (package): 51316-706-07
ndc (product): 51316-706
ndc11 (package): 51316070607
spl id: 50dbb901-6df7-af0b-e063-6394a90acbe3
spl set id: e584a181-1226-5dda-e053-2a95a90ab645

Reported adverse events (FAERS/openFDA)#

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