Centroll NAP ADVANCED Hand Sanitizer Gel

Manufacturer
SUNGIN PHARMA
Effective date
2021-07-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:41:37

Label at a glance#

ProductCentroll NAP ADVANCED Hand Sanitizer Gel
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin. For use when soap and water are not available.

Dosage and administration

■ Place enough product on hands to cover all surfaces. Rub hand together until dry. ■ Apply it in a well-ventilated area. ■ Supervise children under 6 years of age when using this product to avoid swallowing. ■ Avoid direct inhalation of vapors during application. (Headaches and irritation to mucous membranes may occur when directly inhaled.) ■ This product is intended only for hand sanitizing. ■ To prevent conten...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70 %

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin.

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

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or rash occurs. These may be signs of a serious condition.

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 hands to cover all surfaces. Rub hand together until dry.

■ Apply it in a well-ventilated area.

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

■ Avoid direct inhalation of vapors during application. (Headaches and irritation to mucous membranes may occur when directly inhaled.)

■ This product is intended only for hand sanitizing.

■ To prevent contents from drying out and contaminants from entering, close lid completely after use.

■ Keep product in its original container as storing the product in anything other than the original container may result in accidents or cause the integrity of the product to diminish.

■ Do not use over bandages, castings, etc. as irritation may occur.

Other information

OTHER SAFETY INFORMATION

■ Store between 15-30 °C (59-86 °F)

■ Avoid freezing and excessive heat above 40 °C (104 °F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Citric acid, Aminomethylpropanol, Urea, Carbomer homopolymer,Tocopherol acetate, Isopropyl myristate, Glycerin, Dexpanthenol, Glycyrrhiza Glabra (Licorice) Root Extract

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Centroll NAP ADVANCED Hand Sanitizer GelCentroll NAP ADVANCED Hand Sanitizer Gel

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
82037-510-012023-01-30C16284748780-1f386c649-a9e2-0266-e053-dadaa90a7c1a[82037-510-01] [Gel] [Bottle+Pump] [500 mL] Centroll NAP ADVANCED Hand Sanitizer Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82037-510-01Centroll NAP ADVANCED Hand Sanitizer Gel500 mL in 1 BOTTLE, PUMPGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82037-510CENTROLL NAP ADVANCED HAND SANITIZER GEL (ALCOHOL) GEL [SUNGIN PHARMA]1Legacy NDC, 1 package rows20210722_c7aed8cf-bdba-5940-e053-2995a90a881b.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
82037-51082037-510-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
c7aed8cf-bdbb-5940-e053-2995a90a881bc7aed8cf-bdba-5940-e053-2995a90a881b2021-07-21WarningsExact identifier
spl id: c7aed8cf-bdbb-5940-e053-2995a90a881b
spl set id: c7aed8cf-bdba-5940-e053-2995a90a881b

Reported adverse events (FAERS/openFDA)#

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