FDA.reportPublic FDA data

InstantFoam Complete PURE

Manufacturer
SC Johnson Professional USA Inc. | SC Johnson Professional CA Inc.
Effective date
2025-06-20
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:03:47

Label at a glance#

ProductInstantFoam Complete PURE
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

to decrease bacteria on the skin that could cause disease recommended for repeated use

Dosage and administration

Wet hands thouroughly with product and allow to dry without wiping. For children under 6, use only under adult supervision.

Storage and handling

Do not store above 105°F (40°C). May discolor certain fabrics or surfaces. Harmful to wood finishes and plactics.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 80% w/w

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • to decrease bacteria on the skin that could cause disease
  • recommended for repeated use

Warnings

WARNINGS SECTION

For external use only

Flammable: Keep away from fire or flame.

When using this product

OTC - WHEN USING SECTION

  • Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
  • Avoid contact with broken skin.
  • Do not inhale or ingest.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation and redness develop
  • 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 thouroughly with product and allow to dry without wiping.
  • For children under 6, use only under adult supervision.

Other information

STORAGE AND HANDLING SECTION

  • Do not store above 105°F (40°C).
  • May discolor certain fabrics or surfaces.
  • Harmful to wood finishes and plactics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua (Water), BIS-PEG-12 Dimethicone, Citric Acid, Coco-Glucoside, Dihydroxypropyl PEG-5 Linoleammonium Chloride, Glyceryl Oleate, Panthenol, PEG-200 Hydrogenated Glyceryl Palmitate, PEG-7 Glyceryl Cocoate

PRINCIPAL DISPLAY PANEL - 1 L Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SCJ PROFESSIONAL
A Family Company™

NDC 11084-303-27

InstantFOAM™ COMPLETEPURE

BROAD SPECTRUM HAND SANITIZER

Alcohol FOAM Hand Sanitizer - Dye & Perfume-Free | No water required |
Kills up to 99.9999% of many types of common germs

Pat.www.scjp.com/patents

USDA
CERTIFIED
BIOBASED
PRODUCT
PRODUCT 95%

NSF® 1.
Nonfood Compounds
Program Listed E3
152215

UL 2.
ECOLOGO
PRODUCTS CERTIFIED FOR
REDUCED ENVIRONMENTAL
IMPACT. VIEW SPECIFIC
ATTRIBUTES EVALUATED:
UL.COM/EL
UL 2783

1L (33.8 fl oz)

Stock #: IFC1L
4000000691

Manufactured for:
SC Johnson Professional USA, Inc.
Charlotte, NC 28217
1-800-248-7190. www.scjp.com

MADE IN CANADA

deb
SKIN CARE

L-1365 R1/0320

DRUG
FACTS

PRINCIPAL DISPLAY PANEL - 1 L Bottle Label
PRINCIPAL DISPLAY PANEL - 1 L Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1663735ethanol 80 % Topical FoamPSN4
1663735ethanol 0.8 ML/ML Topical FoamSCD4
1663735ethanol 80 % Topical FoamSY4

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11084-303-12InstantFoam Complete PURE1000 mL in 1 BOTTLE, PLASTICLIQUID10004
11084-303-27InstantFoam Complete PURE1000 mL in 1 BOTTLE, PLASTICLIQUID10004
11084-303-40InstantFoam Complete PURE400 mL in 1 BOTTLE, PUMPLIQUID4004
11084-303-66InstantFoam Complete PURE1000 mL in 1 BOTTLE, PLASTICLIQUID10004
11084-303-67InstantFoam Complete PURE1000 mL in 1 CARTRIDGELIQUID10004
11084-303-67InstantFoam Complete PURE1 in 1 KITLIQUID14
11084-303-68InstantFoam Complete PURE2 in 1 BOXLIQUID24
11084-303-68InstantFoam Complete PURE1000 mL in 1 CARTRIDGELIQUID10004

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11084-30311084-303-27, 11084-303-12, 11084-303-40, 11084-303-66, 11084-303-67, 11084-303-68

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
BIS-PEG-12 DIMETHICONE (500 MPA.S)2CNS542YRTIACT
COCO-GLUCOSIDEICS790225BIACT
PEG-7 GLYCERYL COCOATEVNX7251543IACT
GLYCERYL OLEATE4PC054V79PIACT
PANTHENOLWV9CM0O67ZIACT
PEG-200 HYDROGENATED GLYCERYL PALMATEW161T051Y1IACT
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE0Y0NQR2GH1IACT

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
InstantFoam Complete PUREALCOHOLSC Johnson Professional USA Inc.22eaf210-ff25-4bec-a6d4-65c711d2917f2025-06-20WarningsExact identifier
ndc (package): 11084-303-68
ndc (package): 11084-303-12
ndc (package): 11084-303-27
ndc (package): 11084-303-66
ndc (package): 11084-303-67
ndc (package): 11084-303-40
ndc (product): 11084-303
ndc11 (package): 11084030327
ndc11 (package): 11084030366
ndc11 (package): 11084030312
ndc11 (package): 11084030367
ndc11 (package): 11084030368
ndc11 (package): 11084030340
spl id: c90f89f1-bc7d-4c81-89f7-5f7c5353e6b8
spl set id: 22eaf210-ff25-4bec-a6d4-65c711d2917f

Reported adverse events (FAERS/openFDA)#

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