SunDrops 73

Dosage form: soap
Ingredients: Alcohol 650mL in 1L
Labeler: Sunburst Chemicals, Inc.
NDC Code: 63621-355

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.

Drug Facts

Active Ingredient

Ethyl Alcohol 65% v/v

Purpose

Skin Sanitizer

Use

To help reduce the amount of bacteria on 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 a doctor immediately.

Stop use and consult a doctor when skin irritation appears and lasts.

KEEP OUT OF REACH OF CHILDREN.

Directions
  • Pump a small amount of foam into palm of hand.
  • Spread on hands and rub into skin until dry.
  • Pump a smaller amount (2.5 grams) into one hand and spread over both hands and wrists.
  • Rub into skin until dry.
  • Children should be supervised while using this product.

Inactive Ingredients

Water, DEA-C8-18 Perfluoroalkylethyl Phosphate, Glycerin

PRINCIPAL DISPLAY PANEL - Label

SUNBURST CHEMICALS

SunDrops 73

Contains 6 Bottles
Net Contents Each 16 fl. oz. (1 pt.) 500 mL
Total Net Volume 96 fl. oz. (3 qt.) 3 L

SUNDROPS 73 
alcohol soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63621-355
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Alcohol (Alcohol) Alcohol650 mL  in 1 L
Inactive Ingredients
Ingredient NameStrength
WATER 
GLYCERIN 
DIETHANOLAMINE BIS(C8-C18 PERFLUOROALKYLETHYL)PHOSPHATE 
Product Characteristics
Colorwhite (water white - colorless, dispensed as white foam) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:63621-355-506 BOTTLE, PUMP in 1 BOX
10.500 L in 1 BOTTLE, PUMP
2NDC:63621-355-558 BAG in 1 BOX
21 L 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)

Revised: 09/2014
 
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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