King Power Gel Instant Hand Sanitizer

Manufacturer
Zhejiang Beta Industry And Trade Co., Ltd.
Effective date
2020-07-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:21:00

Label at a glance#

ProductKing Power Gel Instant Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Wet hands thoroughly with a small amount of product and rub hands together until dry

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 75%

Purpose

OTC - PURPOSE SECTION

/

INDICATIONS & USAGE SECTION

For hand washing to decrease the bacteria on skin that could cause disease

Warnings

WARNINGS SECTION

Flammable, keep away from fire or flame.
For external use only.

Do not use

OTC - DO NOT USE SECTION

Do not use in the eyes, discontinue use if irritation or redness develops
Consult a doctor or poison Control centerright away.

OTC - WHEN USING SECTION

/

OTC - STOP USE SECTION

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OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach from Children.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with a small amount of product and rub hands together until dry

OTHER SAFETY INFORMATION

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Inactive ingredients

INACTIVE INGREDIENT SECTION

Water(aqua), triethanolamine, aloe barbadensis, aloe vera leaf juice, fragrance, glycerin, propylene, glycol,tocopheryl acetate, vitamin E

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

FDA-Initiated Inactive NDC Indexing#

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
77060-00177060-001-04, 77060-001-02, 77060-001-03, 77060-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
dc721182-fdf8-6ce4-e053-2a95a90a078faab2e2e8-6d3e-545f-e053-2a95a90ab27a2022-04-12WarningsExact identifier
spl set id: aab2e2e8-6d3e-545f-e053-2a95a90ab27a

Reported adverse events (FAERS/openFDA)#

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