MELLOW HAND SANITIZER (ORIGINAL)

Manufacturer
Ningbo Liyuan Daily Chemical Products Co.,Ltd.
Effective date
2017-06-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:15:39

Label at a glance#

ProductMELLOW HAND SANITIZER (ORIGINAL) WITH MOISTURIZER AND VITAMIN E
Active ingredientalcohol
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient                                  Purpose

Ethyl Alcohol                62%      ...        Antiseptic

OTC - PURPOSE SECTION

Hand sanitizer to help decrease bacteria on the skin.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact local poison control center right away.

Children must be supervised in use of this product.

INDICATIONS & USAGE SECTION

keep out of eyes

when water, soap and towel are not available

WARNINGS SECTION

For external use only.
Flammable. Keep away from hear or flame.

Do not apply around eyes; Do not use in ears and mouth. When using this products, avoid contact with eyes. In case of contact, flush eyes with water.

Stop using and ask a doctor, if irritation and redness develops, if condition persists for more than 72 hours, consult a doctor.

DOSAGE & ADMINISTRATION SECTION

Pump as needed into your palms and thoroughly spread on both hands, and rub the skin until dry.

INACTIVE INGREDIENT SECTION

Water, Carbomer, Glycerin, Propylene Glycol, Triethanolamine, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of labelimage of label

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130872711003072GTIN-13: 0872711003072
EAN-13: 0872711003072
GTIN-12: 872711003072
UPC-A: 872711003072
GTIN storage (14 digits): 00872711003072
mellow hand sanitizer original 8 oz.jpg

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76176-30276176-302-01, 76176-302-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
156258ed-f67d-4e27-b051-b6db62d86053a0993a2e-f62d-4e39-93ca-dcdaff5d6c922017-06-16WarningsExact identifier
spl id: 156258ed-f67d-4e27-b051-b6db62d86053
spl set id: a0993a2e-f62d-4e39-93ca-dcdaff5d6c92

Reported adverse events (FAERS/openFDA)#

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