FDA.reportPublic FDA data

Raw Spirit - Moisturizing Hand Sanitizer Foam

Manufacturer
Cosmetic Solutions LLC
Effective date
2020-07-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:21:46

Label at a glance#

ProductRaw Spirit - Moisturizing Hand Sanitizer Foam
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

To decrease bacteria on the skin.

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping - for children under 6, use only under adult supervision - not recommended for infants

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

DRUG FACTS:

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

USES

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin.

WARNINGS

WARNINGS SECTION

For external use only: Hands only.

OTC - WHEN USING SECTION

  • When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. Avoid contact with broken skin.

OTC - STOP USE SECTION

  • Stop use and ask a doctor if irritation or redness develops - condition persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping - for children under 6, use only under adult supervision - not recommended for infants

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water (Aqua), Propanediol, Glycereth-7 Triacetate, Glycerin, Babassu Oil Glycereth-8 Esters, Decyl Glucoside, Calendula Officinalis Flower Extract, Equisetum Arvense Extract, Geranium Maculatum Extract, Honey, Citric Acid, Panax Ginseng Root Extract, Salvia Officinalis Leaf Extract, Sambucus Nigra Flower Extract, Ethylhexylglycerin, Phenoxyethanol, Sodium Hydroxide.

PRINCIPAL DISPLAY PANEL - 120 ml Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

RAW
SPIRIT

moisturizing
antimicrobial
foam

4.1 fl. oz | 120ml

PRINCIPAL DISPLAY PANEL - 120 ml Bottle Label
PRINCIPAL DISPLAY PANEL - 120 ml Bottle Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
66163-1901-12022-01-28C16284748780-1d6a99b39-77b4-a426-e053-dadaa90af4c2Raw Spirit - Moisturizing Hand Sanitizer Foam

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66163-1901-1Raw Spirit - Moisturizing Hand Sanitizer Foam120 mL in 1 BOTTLE, PUMPLIQUID1201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66163-1901RAW SPIRIT - MOISTURIZING HAND SANITIZER FOAM (BENZALKONIUM CHLORIDE) LIQUID [COSMETIC SOLUTIONS LLC]1Legacy NDC, 1 package rows20200717_aacc451e-ff51-4caf-88dc-3a26e4975f0d.zip

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66163-190166163-1901-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
Water059QF0KO0RIACT
Propanediol5965N8W85TIACT
Glycereth-7 TriacetateS9W6Z48HUPIACT
GlycerinPDC6A3C0OXIACT
Babassu Oil Glycereth-8 Esters12XQ76K0YLIACT
Decyl GlucosideZ17H97EA6YIACT
Calendula Officinalis FlowerP0M7O4Y7YDIACT
Equisetum Arvense Branch1L0VKZ185EIACT
Geranium Maculatum Root93IXI5B6OJIACT
HoneyY9H1V576FHIACT
Citric Acid Monohydrate2968PHW8QPIACT
Asian GinsengCUQ3A77YXIIACT
Sambucus Nigra Flower07V4DX094TIACT
Ethylhexylglycerin147D247K3PIACT
PhenoxyethanolHIE492ZZ3TIACT
Sodium Hydroxide55X04QC32IIACT

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
270eff7d-4821-4b2e-9ef5-0e8390ab3d01aacc451e-ff51-4caf-88dc-3a26e4975f0d2020-07-16WarningsExact identifier
spl id: 270eff7d-4821-4b2e-9ef5-0e8390ab3d01
spl set id: aacc451e-ff51-4caf-88dc-3a26e4975f0d

Reported adverse events (FAERS/openFDA)#

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