FDA.reportPublic FDA data

NATURE HAND SANITIZER

Manufacturer
Snt Wholesale, Inc.
Effective date
2020-06-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:18:26

Label at a glance#

ProductNATURE HAND SANITIZER
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

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

Dosage and administration

▪ Apply enough product to cove hand thoroughly. ▪ Rub hands together, until hands feel dry, Do not rinse. ▪ Children under 6 years of age should be supervised when using this product. ▪ Not recommended for infants.

Storage and handling

▪ Store below 105°F (40°C). May discolor some fabrics ▪ Avoid freezing and excessive heat above 105°F (40°C).

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 80% (v/v)

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only: hands

When using this product ▪ Keep out of eyes, ears and mouth. ▪ In case of contact with eyes, rinse eyes thoroughly with water. ▪ Do not inhale or ingest.

Do not use ▪ In children less than 2 months of age. ▪ On open skin wounds.

Stop use and ask a doctor if ▪ Irritation or rash & redness develops. ▪ These may be signs of a serious condition. ▪ Condition persist for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. ▪ If swallowed, get medical help immediately. ▪ Contact a Poison Control Centre right away.

Directions

DOSAGE & ADMINISTRATION SECTION

▪ Apply enough product to cove hand thoroughly. ▪ Rub hands together, until hands feel dry, Do not rinse. ▪ Children under 6 years of age should be supervised when using this product. ▪ Not recommended for infants.

Other information

STORAGE AND HANDLING SECTION

▪ Store below 105°F (40°C). May discolor some fabrics
▪ Avoid freezing and excessive heat above 105°F (40°C).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua (Water), Glycerin, Propylene Glycol, Fragrance (Parfum), Carbomer, Aloe Barbadensis Leaf Extract, Triethanolamine.

SPL UNCLASSIFIED SECTION

Contains 80% Alcohol

Infused with Aloe

Distributed by:

SNT WHOLESALE INC.

5102 Frolich In, Hyattsville,

MD 20781 USA.

Tel: +1-240-423-3875

www.sntwholesale.com

MFG. DT.   : 06/2020

EXP. DT.    : 05/2023

BATCH NO.: HS 038

PLEASE RECYCLE

Made In India

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041498ethanol 80 % Topical GelPSN1
1041498ethanol 0.8 ML/ML Topical GelSCD1
1041498ethanol 80 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78914-000-102022-01-28C16284748780-1d6a99b39-7544-a426-e053-dadaa90af4c2NATURE HAND SANITIZER
78914-000-122022-01-28C16284748780-1d6a99b39-7544-a426-e053-dadaa90af4c2NATURE HAND SANITIZER
78914-000-252022-01-28C16284748780-1d6a99b39-7544-a426-e053-dadaa90af4c2NATURE HAND SANITIZER
78914-000-502022-01-28C16284748780-1d6a99b39-7544-a426-e053-dadaa90af4c2NATURE HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78914-000-10NATURE HAND SANITIZER1000 mL in 1 BOTTLEGEL10001
78914-000-12NATURE HAND SANITIZER120 mL in 1 BOTTLEGEL1201
78914-000-25NATURE HAND SANITIZER250 mL in 1 BOTTLEGEL2501
78914-000-50NATURE HAND SANITIZER500 mL in 1 BOTTLEGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78914-000NATURE HAND SANITIZER (ETHYL ALCOHOL) GEL [SNT WHOLESALE, INC.]1Legacy NDC, 4 package rows20200620_c26ecfd3-8e56-4bcf-b98a-d46dff88a5f1.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78914-00078914-000-12, 78914-000-25, 78914-000-50, 78914-000-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
ALOE VERA LEAFZY81Z83H0XIACT
TROLAMINE9O3K93S3TKIACT

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
7f7edf06-62cb-41ec-8351-7520a44a826ec26ecfd3-8e56-4bcf-b98a-d46dff88a5f12020-06-15WarningsExact identifier
spl id: 7f7edf06-62cb-41ec-8351-7520a44a826e
spl set id: c26ecfd3-8e56-4bcf-b98a-d46dff88a5f1

Reported adverse events (FAERS/openFDA)#

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