Sani-Spritz
Alcohol · Liquid · Topical
Active ingredient
Drug Facts Box OTC-Active Ingredient Section Ethyl Alcohol 62%
Purpose
Drug Facts Box OTC-Purpose Section Antiseptic
Uses
Drug Facts Box OTC-Indications & Usage Section for hand-washing to decrease bacteria on the skin, only when water is not available
Warnings
Drug Facts Box OTC-Warnings Section FLAMMABLE, keep away from fire and flames For external use only
When using this product
Drug Facts Box OTC-When Using Section do not get into eyes if contact occurs, rinse eyes thoroughly with water
Stop use and ask a doctor
Drug Facts Box OTC-Stop Use Section irritation and redness develop
Keep out of reach of children
Drug Facts Box OTC-Keep Out of Reach of Children Section if swallowed, get medical help or contact a Poison Control Center right away
Directions
Drug Facts Box OTC-Dosage & Administration Section press pump twice to deliver two squirts (about a quarter size) of foaming product onto the palm of your hand rub hands together and allow to dry without wiping
Inactive ingredients
Drug Facts Box OTC-Inactive Ingredient Section water, propylene glycol, acid blue 25
Label text from the FDA structured product label by ABC Compounding Co., Inc. (revised Nov 19, 2025). Long sections are shortened; the complete label is on DailyMed.
Active ingredients
- Alcohol in 1 product
Sani-Spritz NDC products (1)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 62257-738 | Alcohol .7 mL/mL Liquid | ABC Compounding Co., Inc. | OTC MONOGRAPH DRUG |
Frequently asked questions
What is Sani-Spritz used for?
Drug Facts Box OTC-Indications & Usage Section for hand-washing to decrease bacteria on the skin, only when water is not available
Who makes Sani-Spritz?
Sani-Spritz is listed by 1 labeler in the FDA NDC directory, including ABC Compounding Co., Inc..