Suzanne Organics Moisturizing Hand Sanitizer

Manufacturer
SLC Skincare
Effective date
2021-05-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:45:17

Label at a glance#

ProductSuzanne Organics Moisturizing Hand Sanitizer
Active ingredientALCOHOL
Label structure6 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin

Dosage and administration

Pump into hands, wetting thoroughly, with produ ct. R ub into skin un til dry. Children under 6 years of age should be supervised by an adult when using this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 64%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from heat and flame.

When using this product

OTC - WHEN USING SECTION

avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or redness develops.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Pump into hands, wetting thoroughly, with produ ct. R ub into skin un til dry.
  • Children under 6 years of age should be supervised by an adult when using this product.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Purified Water (Aqua), Propanediol, Hydroxyethylcellulose, Isopropyl Myristate, Citrus Limonum Oil*, Eugenia Caryophyllus Bud Oil, Eucalyptus Globulus Leaf Oil, Aloe Barbadensis Leaf Juice*, AminoMethyl Propanol, Rosmarinus Officinalis Leaf Oil, Cinnamomum Zeylanicum Bark Oil. *Organic

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

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
15435-20015435-200-04

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 · Source PDF

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
0a218eb6-b201-fa33-e063-6294a90a57d462b3525b-9d41-470c-97f6-89035fbb39d42023-11-14WarningsExact identifier
spl set id: 62b3525b-9d41-470c-97f6-89035fbb39d4

Reported adverse events (FAERS/openFDA)#

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