FDA.reportPublic FDA data

Hand Sanitizing Sprays

Manufacturer
Gemmytec (Shanghai) Co., Ltd | A03 Lab of BTS | Shanghai Chuangshi Industry Group Co., Ltd
Effective date
2020-12-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:36:06

Label at a glance#

ProductHand Sanitizing Sprays
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Spray proper amount of hand sanitizing spray on your hands. Children under 6 years of age should be supervised when using this product.

Storage and handling

Store at 68-77℉ (20-25℃). May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand sanitizing spray to help reduce bacteria on the skin.

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. If case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

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

  • Spray proper amount of hand sanitizing spray on your hands.
  • Children under 6 years of age should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

  • Store at 68-77℉ (20-25℃).
  • May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Fragrance.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

EA-Liq-038EA-Liq-038

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81343-122-012022-01-28C16284748780-1d6a99b39-cf4b-a426-e053-dadaa90af4c2Gemmytec EA 75% LIQ 38mL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81343-122-01Hand Sanitizing Sprays38 mL in 1 BOTTLE, SPRAYLIQUID381

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81343-122HAND SANITIZING SPRAYS (ETHYL ALCOHOL) LIQUID [GEMMYTEC (SHANGHAI) CO., LTD]1Legacy NDC, 1 package rows20201230_b799ca9c-f796-f829-e053-2995a90a4126.zip

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
81343-12281343-122-01

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
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
LEMON OILI9GRO824LLIACT

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
b799ca9c-f797-f829-e053-2995a90a4126b799ca9c-f796-f829-e053-2995a90a41262020-12-29WarningsExact identifier
spl id: b799ca9c-f797-f829-e053-2995a90a4126
spl set id: b799ca9c-f796-f829-e053-2995a90a4126

Reported adverse events (FAERS/openFDA)#

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