Hand Sanitizer

Manufacturer
Jiangsu Ouyali Daily Cosmetic Co., Ltd.
Effective date
2020-04-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:34:22

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Storage and handling

Other Information Do not store above 110°F. May discolor some fabrics.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient
Ethyl Alcohol 75%

OTC - PURPOSE SECTION

Purpose
Antiseptic

INDICATIONS & USAGE SECTION

Uses

For hand washing to decrease bacteria on the skin.

Recommended for repeated use.

WARNINGS SECTION

Warnings

Flammable. Keep away from fire or flame.

For external use only.

Avoid contact with broken skin.

OTC - WHEN USING SECTION

When using this product do not use in or near the eyes.In case of contact, rinse eyes thoroughly with

water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help.

DOSAGE & ADMINISTRATION SECTION

Directions

Not recommended for infants.

Wet hands thoroughly with product and allow to dry without wiping.

Children under 6 years of age should be supervised when using this product.

STORAGE AND HANDLING SECTION

Other Information

Do not store above 110°F. May discolor some fabrics.

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Water, Aloe Barbadensis Leaf Juice, Maltodextrin,Glycerin, Propylene Glycol, Acrylates/C1O-30 Alkyl Acrylate crosspolymer, Triethanoamine, Fragrance, Tocopheryl Acetate.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of bottle labelimage of bottle label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76719-004-012024-12-03C16284748780-1d6a99b39-8a08-a426-e053-dadaa90af4c2a417429e-622c-7c92-e053-2995a90a7a1a
76719-004-012022-01-28C16284748780-1d6a99b39-8a08-a426-e053-dadaa90af4c2a417429e-622c-7c92-e053-2995a90a7a1a

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76719-00476719-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
285eaf0c-19dd-07e1-e063-6394a90a830ea417429e-622c-7c92-e053-2995a90a7a1a2024-12-03WarningsExact identifier
spl set id: a417429e-622c-7c92-e053-2995a90a7a1a

Reported adverse events (FAERS/openFDA)#

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