FDA Label for Sundrops 75
View Indications, Usage & Precautions
Sundrops 75 Product Label
The following document was submitted to the FDA by the labeler of this product Sunburst Chemicals, Inc.. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredient
Ethyl Alcohol 60% v/v
Purpose
Skin Sanitizer
Use
To help reduce amount of bacteria on the skin
Warnings
Flammable. Keep away from fire or flame.
For external use only. If swallowed, seek medical attention.
Otc - When Using
When using this product do not use around or near the eyes. If contact occurs, flush eyes with water and contact doctor immediately.
Otc - Stop Use
Stop use and consult a doctor when skin irritation appears and lasts.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Directions
- Place 5 grams or palmful of product in one hand.
- Spread on hands and rub into skin until dry.
- Place a smaller amount (2.5 grams) in one hand & spread over hands & wrists.
- Rub into skin until dry.
- Supervise children while using this product.
Inactive Ingredients
Water, Glycerin, Fragrance, Carbomer, Propylene Glycol, Diisopropylamine
Package Label.Principal Display Panel
SUNBURST CHEMICALS
SunDrops 75 - 8 fl. oz.
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