FDA.reportPublic FDA data

AQ disposable Antibacterial gel

Manufacturer
Guangzhou Aiqi Biological Technology Co., Ltd.
Effective date
2020-05-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:14:47

Label at a glance#

ProductAQ disposable Antibacterial gel
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

ETHYL alcohol 75% v/v. Purpose: Antibacterial

Purpose

OTC - PURPOSE SECTION

Antibacterial, 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 - 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.

OTC - STOP USE SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

water23.8%,Carbomer0.8%,Triethanolamine0.4%

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

500ml NDC: 78395-001-50

250ml NDC: 78395-001-25

100ml NDC: 78395-001-10

60ml NDC: 78395-001-06

labelslabels

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN1
1305100ethanol 0.75 ML/ML Topical GelSCD1
1305100ethanol 75 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78395-001-062022-01-28C16284748780-1d6a99b39-3ee6-a426-e053-dadaa90af4c2a684cd5d-8101-c682-e053-2a95a90a2810
78395-001-102022-01-28C16284748780-1d6a99b39-3ee6-a426-e053-dadaa90af4c2a684cd5d-8101-c682-e053-2a95a90a2810
78395-001-252022-01-28C16284748780-1d6a99b39-3ee6-a426-e053-dadaa90af4c2a684cd5d-8101-c682-e053-2a95a90a2810
78395-001-502022-01-28C16284748780-1d6a99b39-3ee6-a426-e053-dadaa90af4c2a684cd5d-8101-c682-e053-2a95a90a2810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78395-001-06AQ disposable Antibacterial gel60 mL in 1 BOTTLEGEL601
78395-001-10AQ disposable Antibacterial gel100 mL in 1 BOTTLEGEL1001
78395-001-25AQ disposable Antibacterial gel250 mL in 1 BOTTLEGEL2501
78395-001-50AQ disposable Antibacterial gel500 mL in 1 BOTTLEGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78395-001AQ DISPOSABLE ANTIBACTERIAL GEL (ETHYL ALCOHOL) GEL [GUANGZHOU AIQI BIOLOGICAL TECHNOLOGY CO., LTD.]1Legacy NDC, 4 package rows20200527_a684cd5d-8101-c682-e053-2a95a90a2810.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
78395-00178395-001-06, 78395-001-10, 78395-001-25, 78395-001-50

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
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
TROLAMINE9O3K93S3TKIACT
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
a684c074-cd1c-c6dc-e053-2a95a90ae6e1a684cd5d-8101-c682-e053-2a95a90a28102020-05-25WarningsExact identifier
spl id: a684c074-cd1c-c6dc-e053-2a95a90ae6e1
spl set id: a684cd5d-8101-c682-e053-2a95a90a2810

Reported adverse events (FAERS/openFDA)#

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