SunDrops 75
Alcohol · Gel · Topical
Active ingredient
Active Ingredient Ethyl Alcohol 60% v/v
Purpose
Purpose Skin Sanitizer
Uses
Use To help reduce amount of bacteria on the skin
Warnings
Warnings Flammable. Keep away from fire or flame. For external use only. If swallowed, seek medical attention. When using this product do not use around or near the eyes. If contact occurs, flush eyes with water and contact doctor immediately. Stop use and consult a doctor when skin irritation appears and lasts. Keep out of reach of children.
Keep out of reach of children
Keep out of reach of children.
Directions
Directions Place 5 grams or palmful of product in one hand. Spread on hands and run into skin until dry. Place a smaller amount (2.5 grams) in one hand and spread over both hands and wrists. Rub into skin until dry. Children should be supervised while using this product.
Inactive ingredients
Inactive Ingredients Water, Glycerin, Fragrance, Carbomer, Propylene Glycol, Diisopropylamine
Label text from the FDA structured product label by Sunburst Chemicals, Inc. (revised Nov 11, 2025). Long sections are shortened; the complete label is on DailyMed.
Active ingredients
- Alcohol in 1 product
SunDrops 75 NDC products (1)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 63621-356 | Alcohol .6 mL/mL Gel | Sunburst Chemicals, Inc. | OTC MONOGRAPH DRUG |
Frequently asked questions
What is SunDrops 75 used for?
Use To help reduce amount of bacteria on the skin
Who makes SunDrops 75?
SunDrops 75 is listed by 1 labeler in the FDA NDC directory, including Sunburst Chemicals, Inc..