Aloe Moisturizing Hand

Manufacturer
ShangRao chunyu Technology CO.,LTD.
Effective date
2020-07-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:19:46

Label at a glance#

ProductAloe Moisturizing Hand
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

Pump into hands, wet as needed Lather vigorouslyfor at least 15 seconds Wash skin, rinse thoroughly and dry

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat ab ove 40C (104F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.2%

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

for hand washing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For External Use Only. Avoid contact with eyes. In case of eye contact, flush with water. Do not drink or eat.

Do not use

OTC - DO NOT USE SECTION

/

OTC - WHEN USING SECTION

/

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develops

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Pump into hands, wet as needed
Lather vigorouslyfor at least 15 seconds
Wash skin, rinse thoroughly and dry

Other information

STORAGE AND HANDLING SECTION

Store between 15-30C (59-86F)
Avoid freezing and excessive heat ab ove 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua, Sodium Laureth Sulfate, Cocamide DEA, Cocamidopropyl Betaine, Glycerin, Glycol Distearate, Polyquaternium-7, Sodium chloride, aloe barbadensis Leaf Extract, Disodium EDTA, Citric Acid, Fragrance, DMDM Hydantoin, HC Yellow NO.2, HC Blue NO.2

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

72922-030-01~0672922-030-01~0672922-030-07~1072922-030-07~1072922-030-21~2572922-030-21~2572922-030-11~1672922-030-11~1672922-030-17~2072922-030-17~20

Products#

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NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 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
b8d93b8f-5bb4-8dd5-e053-2a95a90ab8d4aba63c7c-638b-106e-e053-2995a90a2acc2021-01-14WarningsExact identifier
spl set id: aba63c7c-638b-106e-e053-2995a90a2acc

Reported adverse events (FAERS/openFDA)#

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