FDA.reportPublic FDA data

Sweet Skin Etc Hand Sanitizer Wipes

Manufacturer
DOBOLV (QUANZHOU) PAPER CO., LTD
Effective date
2020-10-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:33:22

Label at a glance#

ProductSweet Skin Etc Hand Sanitizer Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

• For hand washing to decrease bacteria on the skin.    Recommended for repeat use.

Dosage and administration

• Wet hands thoroughly with product and allow to dry without rinse. • Children under six years of age should be supervised when using this product.

Storage and handling

• Store in a dry place away from fire.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.10%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Indications and usage

INDICATIONS & USAGE SECTION

• For hand washing to decrease bacteria on the skin. 

  Recommended for repeat use.

Warnings

WARNINGS SECTION

• For external use only.

• Keep out of reach of eyes. If contact occurs, rinse thoroughly with water.

• Do not use if you are allergic to any one of the ingredients.

• Discontinue use if irritation or redness develops, and if condition persists for more than 72 hours consult a physician.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

• Keep out of reach of children unless under adult supervision.

• If swallowed, get medical help.

Directions of use

DOSAGE & ADMINISTRATION SECTION

• Wet hands thoroughly with product and allow to dry without rinse.

• Children under six years of age should be supervised when using this product.

Other Information

STORAGE AND HANDLING SECTION

• Store in a dry place away from fire.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

• Water (Aqua), Glycerol, Propanediol, Aloe Vera Extract, IPBC, Amino acid moisturizer, Vitamin E, Citric acid, Hexadecyl Pyridinium Chloride, Dodecyl polyglucoside.

SPL UNCLASSIFIED SECTION

ALCOHOL FREE

DISTRIBUTED BY

Sweet Skin Etc. , LLC.

Prairieville, LA 70769

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038856benzalkonium Cl 0.1 % Medicated PadPSN1
1038856benzalkonium chloride 1 MG/ML Medicated PadSCD1
1038856benzalkonium chloride 0.1 % Medicated WipesSY1
1038856benzalkonium chloride 0.1 % Topical SwabSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d1c9d1af-bddd-448d-86f7-69052b7d5b47Product name120220627

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79891-002-012022-01-28C16284748780-1d6a99b39-6531-a426-e053-dadaa90af4c2SWEET SKIN etc. HAND SANITIZER Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79891-002-01Sweet Skin Etc Hand Sanitizer Wipes1 in 1 BAGCLOTH11
79891-002-01Sweet Skin Etc Hand Sanitizer Wipes3 mL in 1 PACKAGECLOTH31

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79891-002SWEET SKIN ETC HAND SANITIZER WIPES (BENZALKONIUM CHLORIDE) CLOTH [DOBOLV (QUANZHOU) PAPER CO., LTD]1Legacy NDC, 2 package rows20201111_c90a96e2-184d-420a-9e92-59aba3ac6c78.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79891-00279891-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PROPANEDIOL5965N8W85TIACT
ALOE VERA LEAFZY81Z83H0XIACT
IODOPROPYNYL BUTYLCARBAMATE603P14DHEBIACT
BETAINE3SCV180C9WIACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
CETYLPYRIDINIUM CHLORIDE ANHYDROUS6BR7T22E2SIACT
LAURYL GLUCOSIDE76LN7P7UCUIACT

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
36995c04-99c8-43ae-84c2-322797b96bcdc90a96e2-184d-420a-9e92-59aba3ac6c782020-10-30WarningsExact identifier
spl id: 36995c04-99c8-43ae-84c2-322797b96bcd
spl set id: c90a96e2-184d-420a-9e92-59aba3ac6c78

Reported adverse events (FAERS/openFDA)#

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