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InstantFoam Complete PURE drug information

ALCOHOL
SC Johnson Professional USA Inc. · TOPICAL

Product NDC: 11084-309

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameALCOHOL
Labeler / manufacturerSC Johnson Professional USA Inc.
RouteTOPICAL
Drug classDrug class not supplied in source label
Product NDC11084-309
Label effective date2026-08-27

Official product label reference

InstantFoam Complete PURE — SC Johnson Professional USA Inc.

This page contains 11 source sections for ALCOHOL, topical route. Label set 398ca23c-7202-4670-be14-9829675f7174, version 3.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

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

Purpose

Purpose Antiseptic
Dosage and administration — label text
Directions Wet hands thouroughly with product and allow to dry without wiping. For children under 6, use only under adult supervision.
Warnings
Warnings For external use only Flammable: Keep away from fire or flame. When using this product 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 irritation and redness develop condition persists for more than 72 hours Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Unclassified section
Drug Facts
Active ingredient
Active ingredient Ethyl alcohol 85.6% w/w
While using this medicine
When using this product Keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest.
When to stop use and seek help
Stop use and ask a doctor if irritation and redness develop condition persists for more than 72 hours
Child safety
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Storage and handling
Other information Do not store above 105°F (40°C). May discolor certain fabrics or surfaces. Harmful to wood finishes and plactics.
Inactive ingredient
Inactive ingredients 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

Official sources and product identifiers

Substances listed: ALCOHOL

RxNorm identifiers: 2751495

Package NDC codes

11084-309-66, 11084-309-67, 11084-309-12, 11084-309-40

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.