FDA.reportPublic FDA data

HAND SANITIZER SPARY

Manufacturer
Guangzhou Opseve Cosmetics Co., Ltd
Effective date
2021-11-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:26:23

Label at a glance#

ProductHAND SANITIZER SPARY
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Sealed, stored in a cool, dry place, away from direct sunlight.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

Sealed, stored in a cool, dry place, away from direct sunlight.

Inactive ingredients

INACTIVE INGREDIENT SECTION

fragrance, glycerin, water.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60 mL NDC: 77900-2021-1 Package LabelPackage Label Package LabelPackage Label Package LabelPackage Label Package LabelPackage Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77900-2021-12023-05-05C16284748780-1f386c649-d853-0266-e053-dadaa90a7c1aaded47a9-e689-cede-e053-2995a90a595b
77900-2021-12023-01-30C16284748780-1f386c649-d853-0266-e053-dadaa90a7c1aaded47a9-e689-cede-e053-2995a90a595b

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77900-202177900-2021-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
FRAGRANCE LAVENDER & CHIA F-153480SXS9CO2TZKIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
f672ef12-bc2e-6d6c-e053-2995a90adb62aded47a9-e689-cede-e053-2995a90a595b2023-03-09WarningsExact identifier
spl set id: aded47a9-e689-cede-e053-2995a90a595b

Reported adverse events (FAERS/openFDA)#

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