FDA.reportPublic FDA data

KKW FRAGRANCE

Manufacturer
Hampton Beauty Associates Inc
Effective date
2020-05-26
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:29:00

Label at a glance#

ProductKKW FRAGRANCE 08
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

Put enough product on hands to cover all surfaces and rub hands together until dry. Children under 6 years of age shoud be supervised when using to avoid swallowing.

Storage and handling

store between 15-30C (59-86F). Avoid freezing and excessive heat above 40C (104F).

Label contents#

Full prescribing information#

ACTIVE iNGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v

USE(S)

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that can potentially cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

Flammable keep away from fire or flame. For external use only.When using this product do not use in or near the eyes, ears and mouth. In case of contact with eyes , rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or rash appears. This coud be signs of a serious condition. Keep out of the reach of children. If swallowed get medical help or contact poison control center right away.

Do not use on children less than 2 months of age.

Do not use on open skin wounds.

Directions

DOSAGE & ADMINISTRATION SECTION

Put enough product on hands to cover all surfaces and rub hands together until dry. Children under 6 years of age shoud be supervised when using to avoid swallowing.

other information

STORAGE AND HANDLING SECTION

store between 15-30C (59-86F). Avoid freezing and excessive heat above 40C (104F).

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (aqua), Glycerin, Isopropyl Myristate, Carbomer, Tocophery Acetate, Triethanolamine.

Warnings

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children

Purpose

OTC - PURPOSE SECTION

Antiseptic

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77652-46577652-465-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
AMINOMETHYL PROPANEDIOLCZ7BU4QZJZIACT
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
ETHOHEXADIOLM9JGK7U88VIACT
PHENOXYETHANOLHIE492ZZ3TIACT
WATER059QF0KO0RIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
ALOE VERA LEAFZY81Z83H0XIACT

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
a69528be-1522-d2b1-e053-2995a90ab0d4a57a770d-33bb-0da9-e053-2a95a90aface2020-05-26WarningsExact identifier
spl id: a69528be-1522-d2b1-e053-2995a90ab0d4
spl set id: a57a770d-33bb-0da9-e053-2a95a90aface

Reported adverse events (FAERS/openFDA)#

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