Kellys Delight Hand Sanitizer

Manufacturer
WACO BOTTLING LLC
Effective date
2020-08-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:24:12

Label at a glance#

ProductKellys Delight Hand Sanitizer (Cleanliness)
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

•Wet hands. •Briskly rub hands together until dry. •Supervise children in the use of this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease.

For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from heat or flame.

Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

•Wet hands.

•Briskly rub hands together until dry.

•Supervise children in the use of this product.

Other Information

OTHER SAFETY INFORMATION

•Store at 20-25C(68-77F)

•Avoid freezing and excessive heat above 40C (104F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Fragrance (Parfum), Glycerin, lsopropyl Myristate, PEG-6 & AMP Acrylates I Vinyl lsodecanoate Crosspolymer, Tocopheryl Acetate.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Kellys Delight Cleanliness Hand SanitizerKellys Delight Cleanliness Hand Sanitizer

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79175-008-01Kellys Delight Hand Sanitizer(Cleanliness)59 mL in 1 BOTTLE, PLASTICGEL591
79175-008-02Kellys Delight Hand Sanitizer(Cleanliness)118 mL in 1 BOTTLE, PLASTICGEL1181
79175-008-03Kellys Delight Hand Sanitizer(Cleanliness)236 mL in 1 BOTTLE, PLASTICGEL2361
79175-008-04Kellys Delight Hand Sanitizer(Cleanliness)473 mL in 1 BOTTLE, PLASTICGEL4731
79175-008-05Kellys Delight Hand Sanitizer(Cleanliness)500 mL in 1 BOTTLE, PLASTICGEL5001
79175-008-06Kellys Delight Hand Sanitizer(Cleanliness)946 mL in 1 BOTTLE, PLASTICGEL9461
79175-008-07Kellys Delight Hand Sanitizer(Cleanliness)1000 mL in 1 BOTTLE, PLASTICGEL10001
79175-008-08Kellys Delight Hand Sanitizer(Cleanliness)1893 mL in 1 BOTTLE, PLASTICGEL18931
79175-008-09Kellys Delight Hand Sanitizer(Cleanliness)3785 mL in 1 BOTTLE, PLASTICGEL37851
79175-008-10Kellys Delight Hand Sanitizer(Cleanliness)18927 mL in 1 BOTTLE, PLASTICGEL189271
79175-008-11Kellys Delight Hand Sanitizer(Cleanliness)208198 mL in 1 BOTTLE, PLASTICGEL2081981

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79175-008KELLYS DELIGHT HAND SANITIZER (CLEANLINESS) (ALCOHOL) GEL [WACO BOTTLING LLC]1Legacy NDC, 11 package rows20200808_deb319fa-57b0-425e-ad3e-5fa9e86ee3dd.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

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
6ea9a639-5bd2-4e4e-98a4-fbf013894f0fdeb319fa-57b0-425e-ad3e-5fa9e86ee3dd2020-08-03WarningsExact identifier
spl id: 6ea9a639-5bd2-4e4e-98a4-fbf013894f0f
spl set id: deb319fa-57b0-425e-ad3e-5fa9e86ee3dd

Reported adverse events (FAERS/openFDA)#

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