Sweet skin Hand sanitizer

Manufacturer
Sweet Skin Etc. Llc
Effective date
2023-02-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:54:04

Label at a glance#

ProductSweet skin Hand sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

For hand sanitizing to decrease bacteria on skin Recommended for repeated use

Dosage and administration

Adults and children 2 years and over: apply to hands; allow to dry without wiping. Children under two consult a doctor before usage.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1% Antimicrobial

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • For hand sanitizing to decrease bacteria on skin
  • Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only. Do not use if you are allergic to any of these ingredients

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. In case of contact, flush eyes with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation of redness develops, or if condition proceeds for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children under two consult a doctor before usage.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 2 years and over: apply to hands; allow to dry without wiping.

Children under two consult a doctor before usage.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe 0.1%, glycerol polyether and water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3.785 L NDC: 80958-019-01

ALCOHOL FREE

SWEET

SKIN etc.

HAND SANITIZER

Enriched with ALOE

1 GALLON

PDPPDP

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1049228benzalkonium chloride 0.1 % Topical GelPSN3
1049228benzalkonium chloride 0.001 MG/MG Topical GelSCD3
1049228benzalkonium chloride 0.1 % Topical GelSY3

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80958-001-01Sweet skin Hand sanitizer3.785 L in 1 BOTTLEGEL3.7853

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80958-001SWEET SKIN HAND SANITIZER (BENZALKONIUM CHLORIDE) GEL [SWEET SKIN ETC. LLC]3Legacy NDC, 1 package rows20230214_b215a83c-5aba-e5d3-e053-2a95a90a2ca9.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
80958-00180958-001-01
74621-019

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
f48f9f3a-2160-1b81-e053-2a95a90a12bdb215a83c-5aba-e5d3-e053-2a95a90a2ca92023-02-13WarningsExact identifier
spl id: f48f9f3a-2160-1b81-e053-2a95a90a12bd
spl set id: b215a83c-5aba-e5d3-e053-2a95a90a2ca9

Reported adverse events (FAERS/openFDA)#

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