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SunDrops 75

Medically reviewed on July 20, 2016

Dosage form: gel
Ingredients: Alcohol 0.6mL in 1mL
Labeler: Sunburst Chemicals, Inc.
NDC Code: 63621-356

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

SunDrops 75

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.

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.

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

SUNBURST CHEMICALS

SunDrops 75 - 8 fl. oz.

SUNDROPS 75 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63621-356
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Alcohol (Alcohol) Alcohol0.6 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
GLYCERIN 
PROPYLENE GLYCOL 
DIISOPROPYLAMINE 
CARBOMER INTERPOLYMER TYPE A (55000 CPS) 
Product Characteristics
Colorwhite (water white - colorless, crystal clear) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:63621-356-208 BAG in 1 BOX
11000 mL in 1 BAG
2NDC:63621-356-2512 BOTTLE, PUMP in 1 BOX
2236.6 mL in 1 BOTTLE, PUMP
3NDC:63621-356-306 BAG in 1 BOX
31000 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E10/14/2009
Labeler - Sunburst Chemicals, Inc. (006159339)

 
Sunburst Chemicals, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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