FDA.reportPublic FDA data

Fresh Water

Manufacturer
Spa Dent Inc | Apollo Health and Beauty Care
Effective date
2021-07-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:39:42

Label at a glance#

ProductFresh Water
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

For hand washing to decrease bacteria on the skin.

Dosage and administration

Apply onto dry hands Lather and rinse thoroughly with water.

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

For hand washing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only 

When using this product

OTC - WHEN USING SECTION

Avoid contact with eyes. In case of contact, rinse thoroughly with water. 

Stop use and ask a doctor.

OTC - STOP USE SECTION

If irritation or redness develops and lasts for more than 72 hours

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply onto dry hands
  • Lather and rinse thoroughly with water.

Other Information

STORAGE AND HANDLING SECTION

Store at room temperature

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Cocamidopropyl Betaine, Polysorbate 20, Fragrance (Parfum), Glycerin, Decyl Glucoside, Aloe Barbadensis Leaf Juice, Camellia Sinensis Leaf Extract, Polyquatermium-7, Xanthan Gum, Tetrasodium EDTA, Sodium Citrate, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1 (Cl42090), Ext Violet 2 (Cl 60730)

PDP02

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDP02PDP02

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
79147-02179147-021-02

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
WATER059QF0KO0RIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
POLYSORBATE 207T1F30V5YHIACT
FRAGRANCE CLEAN ORC0600327329LCV5BTFIACT
GLYCERINPDC6A3C0OXIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
ALOE VERA LEAFZY81Z83H0XIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW)0L414VCS5YIACT
XANTHAN GUMTTV12P4NEEIACT
EDETATE SODIUMMP1J8420LUIACT
SODIUM CITRATE1Q73Q2JULRIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
EXT. D&C VIOLET NO. 2G5UX3K0728IACT

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
65d08047-56df-487f-bea2-2e13fee738de5afa4d4e-311b-4063-bb80-c84829cfed312021-07-23WarningsExact identifier
spl id: 65d08047-56df-487f-bea2-2e13fee738de
spl set id: 5afa4d4e-311b-4063-bb80-c84829cfed31

Reported adverse events (FAERS/openFDA)#

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