Refresh AntiBac FOAM

Benzalkonium Chloride · Soap · Topical

Over the counter 1 recall

Active ingredient

Active ingredient BENZALKONIUM CHLORIDE, 0.13%

Purpose

Purpose Antimicrobial

Uses

Uses for handwashing to reduce bacteria on the skin

Warnings

Warnings For external use only When using this product avoid contact with eyes. In case of eye contact, flush with water. Stop use and ask a doctor if irritation and redness develop and persist for more than 3 days. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

When using this product

When using this product avoid contact with eyes. In case of eye contact, flush with water.

Stop use and ask a doctor

Stop use and ask a doctor if irritation and redness develop and persist for more than 3 days.

Keep out of reach of children

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

Directions

Directions apply foaming cleanser to dry hands rub hands together to spread lather wash for 15-20 seconds rinse & dry hands thoroughly

Inactive ingredients

Inactive ingredients AQUA (WATER), GLYCERIN, LAURAMINE OXIDE, BUTYLENE GLYCOL, LACTIC ACID, SALICYLIC ACID, PARFUM (FRAGRANCE), GREEN 5 (CI 61570), YELLOW 5 (CI 19140).

Label text from the FDA structured product label by SC Johnson Professional USA Inc. (revised Aug 13, 2026). Long sections are shortened; the complete label is on DailyMed.

Active ingredients

Refresh AntiBac FOAM NDC products (1)

NDCStrength & formLabelerType
11084-010Benzalkonium Chloride .13 g/L
Soap
SC Johnson Professional USA Inc.OTC MONOGRAPH DRUG

Refresh AntiBac FOAM recalls

Frequently asked questions

What is Refresh AntiBac FOAM used for?

Uses for handwashing to reduce bacteria on the skin

Who makes Refresh AntiBac FOAM?

Refresh AntiBac FOAM is listed by 1 labeler in the FDA NDC directory, including SC Johnson Professional USA Inc..

Has Refresh AntiBac FOAM been recalled?

The FDA enforcement database lists 1 recall for Refresh AntiBac FOAM, most recently D-0220-2019 (class ii): CGMP Deviations: Product was released to market prior to microbiological testing.