FDA Label for Sparkle
View Indications, Usage & Precautions
Sparkle Product Label
The following document was submitted to the FDA by the labeler of this product Nba General Corporation 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(S)
Isopropyl Alcohol 65% v/v. Purpose: Antiseptic
Use
Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Warnings
For external use only. Flammable. Keep away from heat or flame
Do Not Use
- in children less than 2 months of age
- on open skin wounds
Otc - When Using
When using keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash occurs.
Directions
- Place enough product on hands to cover all surfaces. Rub hands together until dry.
Other Information
- Store between 15-30C (59-86F)
- Avoid freezing and excessive heat above 40C (104F)
Inactive Ingredients
glycerin, purified water, carbomer, triethanolamine, fragrance
Otc - 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.
Otc - Purpose
Antiseptic, Hand Sanitizer
Package Label - Principal Display Panel
128 fl oz, 1 gal NDC: 78541-1001-1
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