MELLOW HAND SANITIZER ALOE

Manufacturer
L.e.d. Cosmetics, Inc.
Effective date
2024-12-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:41:55

Label at a glance#

ProductMELLOW HAND SANITIZER ALOE
Active ingredientALCOHOL
Label structure9 sections

Storage and handling

                  • Do not store above 43˚C. May discolor certain fabrics.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol(70%)

Purpose

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

Uses • to decrease bacteria on the skin that could disease

        • recommended for repeated use

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aqua (water), Carbomer, Glycerin, Propylene Glycol, Triethanolamine, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, Parfum, FD&C Yellow No.5, FD&C Blue No.1

DOSAGE & ADMINISTRATION SECTION

Directions • Put a thumbnail size amount in your palm and rub hands briskly until dry.

Note :        • Children under 6 years of age should be supervised during use.

STORAGE AND HANDLING SECTION

                  • Do not store above 43˚C. May discolor certain fabrics.

WARNINGS SECTION

Caution: Flammable. Keep away from fire or flame. For external use only. Keep out of eyes. In case of eye contact, immediately flush with water.

If swallowed, call a physician. Discontinue use if irritation or redness develop. If condition persists for more than 72 hours, consult a physician.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

SPL UNCLASSIFIED SECTION

FORMULA

ETHYL ALCOHOL 70%

Aloe

Vitamin E

Formulated & Developed in Canada

Made in China

Lic.Under Lantern Enterprises Ltd.

Imported for:

Nasco Products Inc.

Richmond, BC. Canada

L.E.D. Cosmetics Inc.

Diamond Bar, CA. USA 91765

Not tested on animals

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN2
582753ethanol 0.7 ML/ML Topical SolutionSCD2
582753ethanol 70 % Topical SolutionSY2
582753ethyl alcohol 70 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77725-005-17MELLOW HAND SANITIZER ALOE500 mL in 1 BOTTLE, PLASTICLIQUID5002
77725-005-81MELLOW HAND SANITIZER ALOE236 mL in 1 BOTTLE, PLASTICLIQUID2362
77725-005-82MELLOW HAND SANITIZER ALOE236 mL in 1 BOTTLE, PLASTICLIQUID2362

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77725-005MELLOW HAND SANITIZER ALOE (ETHYL ALCOHOL) LIQUID [L.E.D. COSMETICS, INC.]2Current NDC, Legacy NDC, 3 package rows20241212_4377ba5e-21f6-407e-9b8c-25e3c6321a5b.zip

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
77725-00577725-005-17, 77725-005-81, 77725-005-82

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
MELLOW HAND SANITIZER ALOEETHYL ALCOHOLL.e.d. Cosmetics, Inc.4377ba5e-21f6-407e-9b8c-25e3c6321a5b2024-12-10WarningsExact identifier
ndc (package): 77725-005-82
ndc (package): 77725-005-81
ndc (package): 77725-005-17
ndc (product): 77725-005
ndc11 (package): 77725000517
ndc11 (package): 77725000582
ndc11 (package): 77725000581
spl id: 04d905d9-2a9c-49a4-a76b-55c68f05159c
spl set id: 4377ba5e-21f6-407e-9b8c-25e3c6321a5b

Reported adverse events (FAERS/openFDA)#

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