FDA.reportPublic FDA data

At Home Signature Collection Hand Sanitizer

Manufacturer
Ganzhou Olivee Cosmetic Co., Ltd.
Effective date
2022-06-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:49:51

Label at a glance#

ProductAt Home Signature Collection Hand Sanitizer Autumn Evening
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Place enough product on your palm to thoroughly cover your hands. Rub hands together briskly until dry. Children under 6 years of age should be supervised when using this product.

Storage and handling

Store below 110°F (43°C). May contain certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% w/w

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Antiseptic cleanser, helps decrease bacteria on skin.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep product away from fire or flame.

When using this product

OTC - WHEN USING SECTION

Avoid contact with the eyes; in case of contact, flush eyes with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Irritation or redness develops and persists.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on your palm to thoroughly cover your hands.
  • Rub hands together briskly until dry.
  • Children under 6 years of age should be supervised when using this product.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Fragrance (Parfum), Aminomethyl Propanol, Aloe Barbadensis Leaf Extract, Tocopheryl Acetate. May contain: Red 33 (CI 17200), Red 4 (CI 14700), Yellow 5 (CI 19140), Blue 1 (CI 42090).

Other information

STORAGE AND HANDLING SECTION

Store below 110°F (43°C). May contain certain fabrics or surfaces.

Questions?

OTC - QUESTIONS SECTION

call 1-800-548-4097

Label 

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of the labelimage of the label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
56136-000-012025-01-30C16284748780-12cef2736-b4ed-d83d-e063-dadaa90ab31fDrug Facts
56136-000-022025-01-30C16284748780-12cef2736-b4ed-d83d-e063-dadaa90ab31fDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
56136-000-01At Home Signature Collection Hand SanitizerAutumn Evening30 mL in 1 BOTTLE, PLASTICGEL301
56136-000-02At Home Signature Collection Hand SanitizerAutumn Evening236 mL in 1 BOTTLE, PLASTICGEL2361

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
56136-000AT HOME SIGNATURE COLLECTION HAND SANITIZER AUTUMN EVENING (ALCOHOL) GEL [GANZHOU OLIVEE COSMETIC CO., LTD.]1Legacy NDC, 2 package rows20220619_65a1a42f-54d3-41a9-b81d-1fbadce8974e.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
56136-00056136-000-01, 56136-000-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROL ACETATE, DL-WR1WPI7EW8IACT
D&C RED NO. 339DBA0SBB0LIACT
FD&C RED NO. 4X3W0AM1JLXIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
FD&C BLUE NO. 1H3R47K3TBDIACT

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
f3d77ca0-62fb-4797-8979-29c7b288c7c065a1a42f-54d3-41a9-b81d-1fbadce8974e2022-06-17WarningsExact identifier
spl id: f3d77ca0-62fb-4797-8979-29c7b288c7c0
spl set id: 65a1a42f-54d3-41a9-b81d-1fbadce8974e

Reported adverse events (FAERS/openFDA)#

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