KNOCK OUT 75% Alcohol hand sanitizer

Manufacturer
Aogrand International Trade Corporation
Effective date
2023-02-11
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:54:01

Label at a glance#

ProductKNOCK OUT 75% Alcohol hand sanitizer
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

hand sanitizer to help decrease bacteria on the skin, when soap and water are not available. recommended for repeated use.

Dosage and administration

place enough product into your palms and thoroughly spread on both hands. rub into skin until dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Uses

INDICATIONS & USAGE SECTION

  • hand sanitizer to help decrease bacteria on the skin, when soap and water are not available.
  • recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire or flame.

Do not apply around eyes. Do not use

OTC - DO NOT USE SECTION

in ears & mouth.

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. In case of contact flush eyes with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

redness or irritation develop and persist for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children must be supervised in use of this product.

Directions

DOSAGE & ADMINISTRATION SECTION

  • place enough product into your palms and thoroughly spread on both hands.
  • rub into skin until dry.

Other information

OTHER SAFETY INFORMATION

  • Store below 110F (43C)
  • May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

carbomer, triethanolamine, water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

500ml NDC: 74621-016-01

KILLS MORE THAN 99% OF GERMS*

KNOCK

OUT

CONTAINS 75% Ethyl Alcohol

HAND SANITIZER

16.9 FL OZ (500ml) Leaves Hands Feeling Soft

*EFFECTIVE AT ELIMINATING 99% OF MANY COMMON HARMFUL GERMS

PDPPDP

1000ml NDC: 74621-016-02

KNOCK

OUT

CONTAINS 75% Ethyl Alcohol

HAND SANITIZER

16.9 FL OZ (500ml) Leaves Hands Feeling Soft

KILLS MORE THAN 99% OF GERMS*

*EFFECTIVE AT ELIMINATING 99% OF MANY COMMON HARMFUL GERMS

PDPPDP

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN3
1305100ethanol 0.75 ML/ML Topical GelSCD3
1305100ethanol 75 % Topical GelSY3

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74621-016-01KNOCK OUT 75% Alcohol hand sanitizer500 mL in 1 BOTTLEGEL5003
74621-016-02KNOCK OUT 75% Alcohol hand sanitizer1000 mL in 1 BOTTLEGEL10003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74621-016KNOCK OUT 75% ALCOHOL HAND SANITIZER (ALCOHOL) GEL [AOGRAND INTERNATIONAL TRADE CORPORATION]3Legacy NDC, 2 package rows20230213_ae1efacb-c0b1-a626-e053-2995a90affa8.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74621-01674621-016-01, 74621-016-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
f47a5c01-5f6c-465e-e053-2a95a90a5465ae1efacb-c0b1-a626-e053-2995a90affa82023-02-11WarningsExact identifier
spl id: f47a5c01-5f6c-465e-e053-2a95a90a5465
spl set id: ae1efacb-c0b1-a626-e053-2995a90affa8

Reported adverse events (FAERS/openFDA)#

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